An 8-year-old boy is brought in for initial evaluation by a pediatrician after he was adopted from an international orphanage. On presentation, he is found to have difficulty with walking as well as bone and joint pain. The adoption papers for the child state that he was the product of a normal birth with no medical issues noted at that time. Since then, he has not seen a doctor until this presentation. Physical exam reveals bowed legs, hard lumps on his ribs, and tenderness to palpation over his bones. He is found to be low in a substance that directly promotes intestinal absorption of a nutrient. Which of the following is a characteristic of the substance that is abnormally low in this patient?
Q22
A 46-year-old man presents to the office complaining of dry, irritated eyes that have gotten worse over the last week. The patient states that he has also developed a red bumpy rash on his arms. On exam, his bilateral cornea and conjunctiva are dry and thickened. There are small ulcerations on the cornea. The skin of the bilateral arms has an erythematous rash characterized by small, white raised lesions. The patient has a history of alcoholism but has no other significant past medical history. What is most likely deficient in this patient?
Q23
A 53-year-old woman presents to her primary care doctor due to discolored, itchy skin, joint pain, and a feeling of abdominal fullness for the past week. Her medical history includes anxiety and depression. She also experiences occasional headaches and dizziness. Of note, the patient recently returned from an expedition to Alaska, where she and her group ate polar bear liver. Physical examination shows dry skin with evidence of excoriation and mild hepatosplenomegaly. Lab investigations reveal an alkaline phosphatase level of 35 U/L and total bilirubin of 0.4 mg/dL. Which of the following tests is most likely to uncover the etiology of her condition?
Q24
An 18-month-old boy is brought to the physician because of a 2-day history of cough, fever, and lethargy. He has been admitted to the hospital twice during the past year for pneumonia. He can stand without support but has not started to walk. He speaks in bisyllables. He is at the 3rd percentile for height and 4th percentile for weight. Examination shows diffuse crackles over bilateral lung fields. Abdominal examination shows hepatosplenomegaly. Fundoscopy shows bright red macular spots. Despite being given appropriate antibiotic therapy, the patient dies. A photomicrograph of a section of the spleen obtained during autopsy is shown. Accumulation of which of the following substances is the most likely cause of this patient's condition?
Q25
A 22-year-old man presents to the physician due to a progressively worsening weakness and an increasingly large abdomen. He notes that he eats well and is fairly active; however, his abdomen has become increasingly protuberant. He also complains of easy bruisability. His medical history is not significant and he takes no medications. Physical examination reveals hepatomegaly and splenomegaly. Several bruises can be seen on the inside of his arms and legs. His skin has a yellowish tinge to it. Laboratory testing shows the following:
Hematocrit 25%
Erythrocyte count 2.5 x 106/mm3
Thrombocyte count 25,000/mm3
A bone marrow biopsy shows a crinkled-paper appearance to the macrophages. Which of the following enzymes is most likely deficient in this patient?
Q26
A 57-year-old woman comes to the physician for a routine examination. She takes no medications. She swims 3 times weekly and jogs several miles with her dog on most mornings. Her diet consists primarily of vegetables, fish, and whole grains; she avoids processed foods and carbohydrates. She drinks one glass of red wine with dinner on most evenings. There is no family history of serious medical illness or cardiovascular disease. Physical examination shows no abnormalities. This patient is most likely to have an increase in which of the following laboratory markers?
Q27
A 12-year-old boy is brought to the emergency department with a hot, swollen, and painful knee. He was playing with his friends and accidentally bumped into one of them with his knee prior to presentation. His medical history is significant for an immunodeficiency syndrome, and he has been treated with long courses of antibiotics for multiple infections. His mother is concerned because he has also had significant bleeding that was hard to control following previous episodes of trauma. Laboratory tests are obtained with the following results:
Prothrombin time: Prolonged
Partial thromboplastin time: Prolonged
Bleeding time: Normal
The activity of which of the following circulating factors would most likely be affected by this patient's disorder?
Q28
A 19-year-old woman with a known history of malabsorption presents with a painful red tongue, red eyes, and cracked lips. She says her symptoms gradually began 4 months ago after moving away from home for college. She also complains of photophobia, spontaneous lacrimation, and itchy dermatitis. Past medical history is significant for a long-standing malabsorption syndrome, which she says that she hasn't been able to maintain her normal diet or take her vitamins regularly due to her busy schedule. The patient is afebrile and vital signs are within normal limits. On physical examination, she has a malnourished appearance with significant pallor. Conjunctival injection is present bilaterally. Which of the following diagnostic tests will be most helpful to support the diagnosis of the most likely vitamin deficiency in this patient?
Q29
A newborn female is found to have ambiguous genitalia and hypotension. Laboratory workup reveals hyperkalemia, hyperreninemia, and elevated levels of 17-hydroxyprogesterone in the patient's urine. Which of the following enzymes would you expect to be deficient in this patient?
Q30
An 8-month-old boy is brought to the physician by his parents for gradually increasing loss of neck control and inability to roll over for the past 2 months. During this time, he has had multiple episodes of unresponsiveness with a blank stare and fluttering of the eyelids. His parents state that he sometimes does not turn when called but gets startled by loud noises. He does not maintain eye contact. He was able to roll over from front to back at 5 months of age and has not yet begun to sit or crawl. His parents are of Ashkenazi Jewish descent. Neurological examination shows generalized hypotonia. Deep tendon reflexes are 3+ bilaterally. Plantar reflex shows extensor response bilaterally. Fundoscopy shows bright red macular spots bilaterally. The remainder of the examination shows no abnormalities. Which of the following is the most likely cause of this patient's symptoms?
Lipid metabolism US Medical PG Practice Questions and MCQs
Question 21: An 8-year-old boy is brought in for initial evaluation by a pediatrician after he was adopted from an international orphanage. On presentation, he is found to have difficulty with walking as well as bone and joint pain. The adoption papers for the child state that he was the product of a normal birth with no medical issues noted at that time. Since then, he has not seen a doctor until this presentation. Physical exam reveals bowed legs, hard lumps on his ribs, and tenderness to palpation over his bones. He is found to be low in a substance that directly promotes intestinal absorption of a nutrient. Which of the following is a characteristic of the substance that is abnormally low in this patient?
A. It is a water soluble vitamin
B. It is produced by parafollicular cells of the thyroid gland
C. It is a fat soluble vitamin (Correct Answer)
D. It is produced by chief cells of the parathyroid gland
E. It is produced by oxyphil cells of the parathyroid gland
Explanation: ***It is a fat soluble vitamin***
- The patient's symptoms (bowed legs, hard lumps on ribs, bone pain, and difficulty walking) are classic signs of **rickets**, caused by severe **vitamin D deficiency**.
- **Vitamin D** is a **fat-soluble vitamin** crucial for intestinal absorption of calcium and phosphate, essential for bone mineralization.
*It is a water soluble vitamin*
- **Water-soluble vitamins** (e.g., B vitamins, vitamin C) are not implicated in the development of rickets or the specific bone abnormalities described.
- Deficiencies in water-soluble vitamins lead to different clinical syndromes, such as scurvy (vitamin C) or beriberi (thiamine).
*It is produced by parafollicular cells of the thyroid gland*
- **Parafollicular C cells** of the thyroid gland produce **calcitonin**, a hormone that lowers blood calcium levels, which is not the substance deficient in this case.
- The low substance is directly involved in absorption, not primarily regulation through calcitonin.
*It is produced by chief cells of the parathyroid gland*
- **Chief cells** of the parathyroid gland produce **parathyroid hormone (PTH)**, which raises blood calcium levels.
- While PTH regulation interacts with vitamin D, PTH itself is not the substance that is abnormally low and directly promotes intestinal absorption of calcium in this patient; rather it would be elevated in severe vitamin D deficiency.
*It is produced by oxyphil cells of the parathyroid gland*
- The function of **oxyphil cells** in the parathyroid gland is not fully understood, but they are generally less numerous than chief cells and are not known to produce a substance directly promoting intestinal nutrient absorption.
- These cells are not associated with vitamin D production or its primary actions.
Question 22: A 46-year-old man presents to the office complaining of dry, irritated eyes that have gotten worse over the last week. The patient states that he has also developed a red bumpy rash on his arms. On exam, his bilateral cornea and conjunctiva are dry and thickened. There are small ulcerations on the cornea. The skin of the bilateral arms has an erythematous rash characterized by small, white raised lesions. The patient has a history of alcoholism but has no other significant past medical history. What is most likely deficient in this patient?
A. Thiamine
B. Folic acid
C. Vitamin B12
D. Vitamin A (Correct Answer)
E. Vitamin K
Explanation: ***Vitamin A***
- **Dry, irritated eyes** with **corneal and conjunctival thickening and ulcerations** are classic signs of **xerophthalmia**, a severe manifestation of **vitamin A deficiency**.
- The **red bumpy rash with small, white raised lesions** on the arms (follicular hyperkeratosis or **phrynoderma**) is also characteristic of **vitamin A deficiency**, commonly seen in individuals with **alcoholism** due to poor nutrition and malabsorption.
*Thiamine*
- **Thiamine (B1) deficiency** (beriberi or Wernicke-Korsakoff syndrome) primarily affects the **nervous and cardiovascular systems**, leading to symptoms like peripheral neuropathy, Wernicke's encephalopathy, or heart failure.
- It does not typically cause the specific ocular or dermatological findings described in this patient.
*Folic acid*
- **Folic acid deficiency** usually presents with **macrocytic anemia**, fatigue, and glossitis.
- It is not associated with the ocular and skin manifestations seen in this patient.
*Vitamin B12*
- **Vitamin B12 deficiency** can cause **macrocytic anemia** and neurological symptoms such as peripheral neuropathy, cognitive impairment, and subacute combined degeneration of the spinal cord.
- It does not explain the specific eye and skin symptoms observed.
*Vitamin K*
- **Vitamin K deficiency** primarily leads to **coagulopathy** (bleeding disorders) due to impaired synthesis of clotting factors.
- It does not cause the ocular dryness, corneal damage, or the specific rash described in the patient.
Question 23: A 53-year-old woman presents to her primary care doctor due to discolored, itchy skin, joint pain, and a feeling of abdominal fullness for the past week. Her medical history includes anxiety and depression. She also experiences occasional headaches and dizziness. Of note, the patient recently returned from an expedition to Alaska, where she and her group ate polar bear liver. Physical examination shows dry skin with evidence of excoriation and mild hepatosplenomegaly. Lab investigations reveal an alkaline phosphatase level of 35 U/L and total bilirubin of 0.4 mg/dL. Which of the following tests is most likely to uncover the etiology of her condition?
A. Jejunal biopsy
B. Plasma retinol levels (Correct Answer)
C. BRCA2 gene mutation
D. Antimitochondrial antibodies
E. Elevated hepatic venous pressure gradient
Explanation: ***Plasma retinol levels***
- The patient's history of consuming **polar bear liver**, combined with symptoms like **discolored, itchy skin**, **joint pain**, and **hepatosplenomegaly**, strongly suggests **vitamin A toxicity (hypervitaminosis A)**.
- Measuring **plasma retinol levels** directly assesses vitamin A status and would confirm dangerously high levels.
*Jejunal biopsy*
- A jejunal biopsy is typically used to diagnose malabsorption syndromes or inflammatory bowel diseases affecting the small intestine.
- The symptoms and the recent dietary history do not point towards a primary intestinal pathology requiring a biopsy for diagnosis.
*BRCA2 gene mutation*
- The BRCA2 gene mutation is associated with an increased risk of certain cancers, particularly breast and ovarian cancers.
- This genetic test is irrelevant to the acute presentation of symptoms or the suspected etiology of vitamin A toxicity.
*Antimitochondrial antibodies*
- **Antimitochondrial antibodies (AMA)** are a hallmark of **primary biliary cholangitis (PBC)**, an autoimmune liver disease.
- While PBC can cause pruritus and liver abnormalities, the patient's acute onset of symptoms after consuming polar bear liver makes vitamin A toxicity a more plausible diagnosis.
*Elevated hepatic venous pressure gradient*
- An **elevated hepatic venous pressure gradient (HVPG)** is a measure of portal hypertension and is used to assess the severity of liver cirrhosis.
- While hepatomegaly is present, there is no indication of advanced liver disease or portal hypertension in the initial presentation; the liver enzyme levels (ALP, bilirubin) are normal, which contradicts severe liver damage leading to portal hypertension.
Question 24: An 18-month-old boy is brought to the physician because of a 2-day history of cough, fever, and lethargy. He has been admitted to the hospital twice during the past year for pneumonia. He can stand without support but has not started to walk. He speaks in bisyllables. He is at the 3rd percentile for height and 4th percentile for weight. Examination shows diffuse crackles over bilateral lung fields. Abdominal examination shows hepatosplenomegaly. Fundoscopy shows bright red macular spots. Despite being given appropriate antibiotic therapy, the patient dies. A photomicrograph of a section of the spleen obtained during autopsy is shown. Accumulation of which of the following substances is the most likely cause of this patient's condition?
A. Ceramide trihexoside
B. Cerebroside sulfate
C. Glucocerebroside
D. Sphingomyelin (Correct Answer)
E. Limit dextrin
Explanation: ***Sphingomyelin***
- The patient's history of **recurrent pneumonia**, **hepatosplenomegaly**, **developmental delay** (not walking, bisyllables at 18 months), **failure to thrive**, and **cherry-red macular spots** (on fundoscopy) are classic signs of **Niemann-Pick disease**.
- **Niemann-Pick disease** is an autosomal recessive lysosomal storage disorder caused by a deficiency of the enzyme **acid sphingomyelinase**, leading to the accumulation of **sphingomyelin** in various tissues.
*Ceramide trihexoside*
- Accumulation of **ceramide trihexoside** is characteristic of **Fabry disease**, an X-linked recessive lysosomal storage disorder.
- While Fabry disease can cause renal failure, angiokeratomas, and peripheral neuropathy, it does not typically present with **hepatosplenomegaly**, **recurrent pneumonia**, or **cherry-red macular spots** in infancy.
*Cerebroside sulfate*
- Accumulation of **cerebroside sulfate** (sulfatide) is characteristic of **metachromatic leukodystrophy**, an autosomal recessive lysosomal storage disorder.
- This condition primarily affects the **nervous system**, leading to demyelination and neurological deterioration, but it does not present with **hepatosplenomegaly** or **cherry-red macula**.
*Glucocerebroside*
- Accumulation of **glucocerebroside** is characteristic of **Gaucher disease**, an autosomal recessive lysosomal storage disorder.
- While Gaucher disease causes **hepatosplenomegaly** and can lead to bone crises, it does not typically present with **cherry-red macular spots**, severe early developmental delay, or recurrent pulmonary infections in the same manner as Niemann-Pick.
*Limit dextrin*
- Accumulation of **limit dextrin** is associated with **Cori disease** (Type III glycogen storage disease).
- This disorder primarily affects the **liver** and **muscles**, causing hepatomegaly, hypoglycemia, and myopathy, but it does not present with **cherry-red macular spots** or specific developmental delays and recurrent infections seen in this patient.
Question 25: A 22-year-old man presents to the physician due to a progressively worsening weakness and an increasingly large abdomen. He notes that he eats well and is fairly active; however, his abdomen has become increasingly protuberant. He also complains of easy bruisability. His medical history is not significant and he takes no medications. Physical examination reveals hepatomegaly and splenomegaly. Several bruises can be seen on the inside of his arms and legs. His skin has a yellowish tinge to it. Laboratory testing shows the following:
Hematocrit 25%
Erythrocyte count 2.5 x 106/mm3
Thrombocyte count 25,000/mm3
A bone marrow biopsy shows a crinkled-paper appearance to the macrophages. Which of the following enzymes is most likely deficient in this patient?
A. Arylsulfatase A
B. Sphingomyelinase
C. α-galactosidase
D. Hexosaminidase
E. β-glucosidase (Correct Answer)
Explanation: ***β-glucosidase***
- The patient's symptoms (hepatosplenomegaly, easy bruisability, anemia, thrombocytopenia) and the characteristic **crinkled-paper appearance of macrophages** on bone marrow biopsy are pathognomonic for **Gaucher disease**.
- **Gaucher disease** is an autosomal recessive lysosomal storage disorder caused by a deficiency of the enzyme **β-glucosidase** (also known as glucocerebrosidase), leading to the accumulation of glucocerebroside.
*Arylsulfatase A*
- Deficiency of **arylsulfatase A** causes **metachromatic leukodystrophy**, characterized by progressive demyelination and neurological symptoms, not the hematological and visceral findings seen here.
- While it is also a lysosomal storage disorder, the clinical presentation and specific cell morphology are distinct.
*Sphingomyelinase*
- Deficiency of **sphingomyelinase** leads to **Niemann-Pick disease**, which shares some features with Gaucher disease, such as hepatosplenomegaly.
- However, the characteristic cell found in Niemann-Pick disease is a lipid-laden macrophage with a **foamy appearance**, not a "crinkled-paper" appearance.
*α-galactosidase*
- Deficiency of **α-galactosidase A** causes **Fabry disease**, an X-linked lysosomal storage disorder.
- Symptoms include episodic pain, acroparesthesias, angiokeratomas, and renal/cardiac involvement, which are not described in this patient.
*Hexosaminidase*
- Deficiency of **hexosaminidase A** causes **Tay-Sachs disease**, a lysosomal storage disorder primarily affecting the central nervous system.
- It is characterized by progressive neurodegeneration, developmental delay, and a **cherry-red spot** on the retina, without the hepatosplenomegaly or characteristic macrophages seen in this case.
Question 26: A 57-year-old woman comes to the physician for a routine examination. She takes no medications. She swims 3 times weekly and jogs several miles with her dog on most mornings. Her diet consists primarily of vegetables, fish, and whole grains; she avoids processed foods and carbohydrates. She drinks one glass of red wine with dinner on most evenings. There is no family history of serious medical illness or cardiovascular disease. Physical examination shows no abnormalities. This patient is most likely to have an increase in which of the following laboratory markers?
A. Low density lipoprotein
B. Apolipoprotein B-100
C. Very low density lipoprotein
D. Triglyceride
E. High density lipoprotein (Correct Answer)
Explanation: ***High density lipoprotein***
- This patient's lifestyle, characterized by **regular exercise**, a **diet rich in good fats** (fish, whole grains), and **moderate alcohol consumption** (one glass of red wine), are all factors known to increase **HDL levels**.
- **HDL** is often referred to as "good cholesterol" and plays a vital role in reverse cholesterol transport, removing cholesterol from peripheral tissues and transporting it to the liver for excretion.
*Low density lipoprotein*
- A diet high in fruits, vegetables, fish, and whole grains, along with regular exercise, would typically lead to a **decrease in LDL** ("bad cholesterol").
- The absence of processed foods and carbohydrates further supports a **lower, not higher, LDL level**.
*Apolipoprotein B-100*
- **Apolipoprotein B-100** is the primary protein component of LDL and VLDL, and its levels generally **correlate directly with LDL levels**.
- Given the patient's healthy lifestyle, an increase in LDL is unlikely, making an increase in **ApoB-100** also unlikely.
*Very low density lipoprotein*
- VLDL levels are strongly influenced by dietary intake, particularly of **saturated fats and refined carbohydrates**.
- This patient's diet explicitly avoids processed foods and carbohydrates, making an **increase in VLDL unlikely**.
*Triglyceride*
- This patient's **healthy diet**, including lean proteins and whole grains, combined with regular exercise and limited saturated fats, would typically result in **lower triglyceride levels**.
- **Moderate alcohol intake** may temporarily increase triglycerides in some individuals, but the overall lifestyle factors strongly point towards reduced levels.
Question 27: A 12-year-old boy is brought to the emergency department with a hot, swollen, and painful knee. He was playing with his friends and accidentally bumped into one of them with his knee prior to presentation. His medical history is significant for an immunodeficiency syndrome, and he has been treated with long courses of antibiotics for multiple infections. His mother is concerned because he has also had significant bleeding that was hard to control following previous episodes of trauma. Laboratory tests are obtained with the following results:
Prothrombin time: Prolonged
Partial thromboplastin time: Prolonged
Bleeding time: Normal
The activity of which of the following circulating factors would most likely be affected by this patient's disorder?
A. von Willebrand factor
B. Factor VIII
C. Factor X (Correct Answer)
D. Protein C
E. Factor XI
Explanation: ***Factor X***
- This patient presents with **vitamin K deficiency** secondary to long-term antibiotic use, which disrupts gut flora responsible for vitamin K synthesis.
- **Factor X** is a vitamin K-dependent procoagulant factor essential for both the intrinsic and extrinsic coagulation pathways (common pathway).
- Vitamin K deficiency leads to reduced activity of **all vitamin K-dependent factors** (II, VII, IX, X, Protein C, Protein S), but the **bleeding presentation** is caused by deficiency of the **procoagulant factors** (II, VII, IX, X).
- Factor X deficiency results in **prolonged PT and PTT** (affects both pathways) with **normal bleeding time** (platelet function intact), exactly matching this patient's lab findings.
- The clinical presentation of **hemarthrosis and significant bleeding** following trauma is consistent with a coagulation factor deficiency, specifically Factor X in the context of vitamin K deficiency.
*Factor XI*
- Factor XI deficiency (Hemophilia C) would cause a **prolonged PTT only**, not prolonged PT.
- This patient has **both prolonged PT and PTT**, ruling out isolated Factor XI deficiency.
*von Willebrand factor*
- von Willebrand factor deficiency primarily causes **prolonged bleeding time** due to impaired platelet adhesion.
- This patient has **normal bleeding time**, making von Willebrand disease unlikely.
*Factor VIII*
- Factor VIII deficiency (Hemophilia A) causes **prolonged PTT only** with normal PT.
- The patient's **prolonged PT and PTT** excludes isolated Factor VIII deficiency.
*Protein C*
- Protein C is a vitamin K-dependent **anticoagulant** factor, so its activity would indeed be reduced in vitamin K deficiency.
- However, Protein C deficiency causes **thrombosis** (increased clotting), not bleeding.
- This patient presents with **bleeding** and prolonged coagulation times, which are caused by deficiency of **procoagulant factors** like Factor X, not anticoagulant factors like Protein C.
- While Protein C activity is affected by vitamin K deficiency, it does not explain the patient's bleeding presentation.
Question 28: A 19-year-old woman with a known history of malabsorption presents with a painful red tongue, red eyes, and cracked lips. She says her symptoms gradually began 4 months ago after moving away from home for college. She also complains of photophobia, spontaneous lacrimation, and itchy dermatitis. Past medical history is significant for a long-standing malabsorption syndrome, which she says that she hasn't been able to maintain her normal diet or take her vitamins regularly due to her busy schedule. The patient is afebrile and vital signs are within normal limits. On physical examination, she has a malnourished appearance with significant pallor. Conjunctival injection is present bilaterally. Which of the following diagnostic tests will be most helpful to support the diagnosis of the most likely vitamin deficiency in this patient?
A. Measurement of erythrocyte folate levels
B. Measurement of erythrocyte glutathione reductase activity (Correct Answer)
C. Measurement of erythrocyte glutamic oxaloacetic transaminase activity
D. Measurement of erythrocyte transketolase activity
E. Measurement of serum methylmalonic acid levels
Explanation: ***Measurement of erythrocyte glutathione reductase activity***
- This measures the activity of an enzyme that requires **flavin adenine dinucleotide (FAD)**, a coenzyme derived from **riboflavin (vitamin B2)**. Reduced activity, especially after FAD stimulation, suggests **riboflavin deficiency**.
- The patient's symptoms (painful red tongue, red eyes, cracked lips, photophobia, spontaneous lacrimation, itchy dermatitis) are classic manifestations of **ariboflavinosis**, exacerbated by her history of malabsorption and poor dietary intake.
*Measurement of erythrocyte folate levels*
- This test is used to diagnose **folate (vitamin B9) deficiency**, which can cause **macrocytic anemia** and megaloblastic changes.
- While malabsorption can lead to folate deficiency, the patient's specific constellation of symptoms (cheilosis, glossitis, angular stomatitis, ocular symptoms) is more indicative of **riboflavin deficiency**, not folate.
*Measurement of erythrocyte glutamic oxaloacetic transaminase activity*
- This (also known as AST or Aspartate Aminotransferase) enzyme requires **pyridoxal phosphate (vitamin B6)** as a coenzyme. Measurement of its activity, particularly with and without B6 supplementation, can assess **vitamin B6 status**.
- While B6 deficiency can present with dermatitis and glossitis, the prominent ocular symptoms and cheilosis point more strongly towards **riboflavin deficiency**.
*Measurement of erythrocyte transketolase activity*
- This test assesses **thiamine (vitamin B1) status**, as transketolase requires **thiamine pyrophosphate (TPP)** as a cofactor. Reduced activity, especially after TPP stimulation, indicates **thiamine deficiency (beri-beri)**.
- Thiamine deficiency typically presents with neurological symptoms (dry beri-beri) or cardiovascular symptoms (wet beri-beri), which are not described in this patient's presentation.
*Measurement of serum methylmalonic acid levels*
- Elevated **methylmalonic acid (MMA)** levels in serum are a highly sensitive and specific indicator of **vitamin B12 deficiency**, as B12 is essential for the conversion of MMA to succinyl CoA.
- While vitamin B12 deficiency can cause glossitis and neurological symptoms, the patient's specific ocular and dermatological findings are not characteristic of B12 deficiency.
Question 29: A newborn female is found to have ambiguous genitalia and hypotension. Laboratory workup reveals hyperkalemia, hyperreninemia, and elevated levels of 17-hydroxyprogesterone in the patient's urine. Which of the following enzymes would you expect to be deficient in this patient?
A. 11-hydroxylase
B. 3β-hydroxysteroid dehydrogenase
C. 11β-hydroxysteroid dehydrogenase
D. 21-hydroxylase (Correct Answer)
E. 17-hydroxylase
Explanation: ***21-hydroxylase***
- **21-hydroxylase deficiency** is the most common cause of **congenital adrenal hyperplasia (CAH)**, leading to a build-up of **17-hydroxyprogesterone** and its metabolites, which are shunted into androgen pathways.
- The deficiency in cortisol and aldosterone synthesis results in **hyponatremia**, **hyperkalemia**, and **hypotension** (due to salt-wasting) and **ambiguous genitalia** in females due to excess androgens.
*11-hydroxylase*
- **11-hydroxylase deficiency** also causes **CAH** and leads to ambiguous genitalia in females, but it is typically associated with **hypertension** due to the accumulation of 11-deoxycorticosterone, a mineralocorticoid, not hypotension.
- While 17-hydroxyprogesterone might be elevated, the defining feature of this deficiency is elevated levels of **11-deoxycorticosterone** and **11-deoxycortisol**.
*3β-hydroxysteroid dehydrogenase*
- **3β-hydroxysteroid dehydrogenase deficiency** leads to impaired synthesis of all adrenal steroids (glucocorticoids, mineralocorticoids, and androgens), resulting in severe **salt-wasting** and **hypotension**.
- However, females with this deficiency would typically present with **undervirilized** or normal genitalia, rather than ambiguous genitalia, due to reduced androgen synthesis.
*11β-hydroxysteroid dehydrogenase*
- **11β-hydroxysteroid dehydrogenase deficiency** is typically associated with **apparent mineralocorticoid excess syndrome**, leading to **hypertension** and **hypokalemia**, not hyperkalemia or ambiguous genitalia.
- This enzyme is responsible for converting cortisol to cortisone, preventing cortisol from activating mineralocorticoid receptors.
*17-hydroxylase*
- **17-hydroxylase deficiency** impairs the synthesis of sex hormones and cortisol, leading to **hypertension** and **hypokalemia** due to increased mineralocorticoid production (e.g., corticosterone, 11-deoxycorticosterone).
- Females would typically have **normal female external genitalia** but lack pubertal development, and males would present with **undervirilized external genitalia**.
Question 30: An 8-month-old boy is brought to the physician by his parents for gradually increasing loss of neck control and inability to roll over for the past 2 months. During this time, he has had multiple episodes of unresponsiveness with a blank stare and fluttering of the eyelids. His parents state that he sometimes does not turn when called but gets startled by loud noises. He does not maintain eye contact. He was able to roll over from front to back at 5 months of age and has not yet begun to sit or crawl. His parents are of Ashkenazi Jewish descent. Neurological examination shows generalized hypotonia. Deep tendon reflexes are 3+ bilaterally. Plantar reflex shows extensor response bilaterally. Fundoscopy shows bright red macular spots bilaterally. The remainder of the examination shows no abnormalities. Which of the following is the most likely cause of this patient's symptoms?
A. Sphingomyelinase deficiency
B. β-glucocerebrosidase deficiency
C. α-galactosidase A deficiency
D. ATP-binding cassette transporter mutation
E. β-hexosaminidase A deficiency (Correct Answer)
Explanation: ***β-hexosaminidase A deficiency***
- The constellation of **developmental regression** (loss of neck control, inability to roll over), **hypotonia**, **exaggerated startle response**, **cherry-red macular spots**, and **Ashkenazi Jewish descent** is classic for **Tay-Sachs disease**, which is caused by a deficiency in β-hexosaminidase A.
- The patient's seizures ("unresponsiveness with a blank stare and fluttering of the eyelids") and **hyperreflexia** (3+ deep tendon reflexes, extensor plantar response) are also consistent with the progressive neurodegeneration seen in Tay-Sachs disease.
*Sphingomyelinase deficiency*
- This deficiency causes **Niemann-Pick disease**, which can also present with **developmental regression**, **hypotonia**, and **cherry-red macular spots**.
- However, Niemann-Pick disease typically involves **hepatosplenomegaly** and **pulmonary involvement**, which are not mentioned in this patient's presentation.
*β-glucocerebrosidase deficiency*
- This deficiency leads to **Gaucher disease**, characterized by **hepatosplenomegaly**, **bone crises**, and cytopenias.
- While some forms can have neurological symptoms, the classic cherry-red spot and pronounced developmental regression as described are not typical of Gaucher disease.
*α-galactosidase A deficiency*
- This deficiency causes **Fabry disease**, which is an **X-linked lysosomal storage disorder** presenting with **neuropathic pain**, **angiokeratomas**, **renal disease**, and **cardiac involvement** in adolescence or adulthood.
- It does not present with infantile neurodegeneration or cherry-red spots.
*ATP-binding cassette transporter mutation*
- Mutations in ABC transporters can lead to various disorders, such as **adrenoleukodystrophy** (deficiency in VLCFA transport) or **cystic fibrosis**.
- These conditions do not present with the specific combination of symptoms, especially the cherry-red macula and profound developmental regression, seen in this infant.