A 24-year-old man presents to the emergency department complaining of a prolonged course of diarrhea. He reports that he has had 3–4 large volume watery stools daily for the last several weeks. He has no pain with bowel movements, no abdominal pain, and no blood in his stools. He is homeless and uses recreational drugs. He also reports that he usually drinks a half-liter of whiskey, or whatever else he can find, every day and he has done this for several years. The physical exam is notable for a hyperpigmented rash across his face, neck, chest, and the backs of his hands and forearms. On mental status exam, he is oriented to person and place but not time; he scores a 23/30 on the Montreal Cognitive Assessment (MOCA). This patient's presentation is most likely related to which of the following micronutrients?
Q62
A 6-month-old boy is brought to the emergency department by his mother because of recurrent vomiting and yellowing of his eyes. The mother says that he has been eating poorly since she started weaning him off of breast milk 5 days ago. At this time, mashed vegetables and fruits were added to his diet. Examination shows scleral jaundice and dry mucous membranes. The tip of the liver is palpable 4 cm below the right costal margin. His serum glucose concentration is 47 mg/dL, serum alanine aminotransferase is 55 U/L, and serum aspartate aminotransferase is 66 U/L. Which of the following enzymes is most likely deficient?
Q63
A 2-year-old boy is brought to the emergency department by his mother 30 minutes after having a generalized tonic-clonic seizure. He was born at home and has not attended any well-child visits. He is not yet able to walk and does not use recognizable words. His paternal uncle has a severe intellectual disability and has been living in an assisted-living facility all of his life. The boy's urine phenylacetate level is markedly elevated. Which of the following amino acids is most likely nutritionally essential for this patient because of his underlying condition?
Q64
A 4-month-old boy is brought to the physician because of a seizure. He was delivered at term after an uncomplicated pregnancy. He is currently at the 10th percentile for height, 5th percentile for weight, and 15th percentile for head circumference. Examination shows muscle hypotonia. His serum lactic acid and alanine are elevated. A functional assay of pyruvate dehydrogenase complex in serum leukocytes shows decreased enzyme activity. Supplementation with which of the following substances should be avoided in this patient?
Q65
A 3-month-old boy is brought to the pediatrician by his mother after she notices orange sand–like crystalline material in her child’s diaper. He is not currently taking any medication and is exclusively breastfed. His immunizations are up to date. The doctor tells the mother that her son may have an X-linked recessive disorder. The boy is prescribed a medication that inhibits an enzyme responsible for the production of the crystals seen in his urine microscopy. Which of the following enzymes is the target of this medication?
Q66
You have isolated cells from a patient with an unknown disorder and would like to locate the defect in this patient. When radiolabeled propionate is added to the mitochondria, no radiolabeled carbon dioxide is detected. However, when radiolabeled methylmalonic acid is added, radiolabeled carbon dioxide is detected from these cells. Which of the following amino acids can be fully metabolized by this patient?
Q67
A 53-year-old homeless woman is brought to the emergency department by the police after she was found in the park lying unconscious on the ground. Both of her pupils are normal in size and reactive to light. There are no signs of head trauma. Finger prick test shows a blood glucose level of 20 mg/dL. She has been brought to the emergency department for acute alcohol intoxication several times before. Her vitals signs include: blood pressure 100/70 mm Hg, heart rate 90/min, respiratory rate 22/min, and temperature 35.0℃ (95.0℉). On general examination, she looks pale, but there is no sign of icterus noted. On physical examination, the abdomen is soft and non-tender and no hepatosplenomegaly noted. She spontaneously opens her eyes after the administration of a bolus of intravenous dextrose, thiamine, and naloxone. Blood and urine samples are drawn for toxicology screening. Finally, the blood alcohol level turns out to be 300 mg/dL. What will be the most likely laboratory findings in this patient?
Q68
A 25-year-old woman presents her physician with a complaint of feeling tired and low on energy for the past 6 months. She also has noticed she has been having trouble performing daily tasks and at times experiencing near-fainting spells. She has no recollection of similar instances in the past. Her past medical history is insignificant, except for the fact that she has been a strict vegan for the last 5 years. Her vital signs are stable. On physical examination, she is visibly pale and has decreased position and vibratory sensation in her both lower extremities. There is decreased lower limb reflexes with sensation intact. A complete blood count - done last week, - shows hemoglobin of 9.7 g/dL with an MCV of 110 fL. The serum levels of which of the following will most likely aid in the physician’s treatment plan?
Q69
A 25-year-old woman presents to the emergency department for the evaluation of a severe abdominal pain of 5 hours duration. The pain is colicky but is not localized. She also complains of nausea and an episode of vomiting. For the past 2 days, she has been constipated. She has had similar episodes of varying intensity in the past that resolved over a few hours. Several laboratory tests and imaging studies have been conducted in the past which were all within normal limits. The medical history is otherwise unremarkable. She denies smoking cigarettes or drinking alcohol. The vital signs are as follows: pulse 100/min, respiratory rate 16/min, and blood pressure 138/84 mm Hg. The physical examination reveals a young woman in obvious distress. There is no tenderness on abdominal examination. Laboratory tests are ordered, analgesics are administered, and the patient was admitted overnight for observation. In the morning, a urine sample was shown to have darkened overnight. Abnormal levels of which of the following most likely led to this patient’s condition?
Q70
A 14-year-old boy is brought to the physician by his mother because of a 12-hour history of abdominal pain and dark urine. Three days ago, he developed a cough, sore throat, and rhinorrhea. Examination shows conjunctival pallor, scleral icterus, and mild splenomegaly. A peripheral blood smear shows small round inclusions within erythrocytes and several erythrocytes with semicircular indentations. The underlying cause of this patient's condition is most likely to also affect which of the following processes?
Metabolism US Medical PG Practice Questions and MCQs
Question 61: A 24-year-old man presents to the emergency department complaining of a prolonged course of diarrhea. He reports that he has had 3–4 large volume watery stools daily for the last several weeks. He has no pain with bowel movements, no abdominal pain, and no blood in his stools. He is homeless and uses recreational drugs. He also reports that he usually drinks a half-liter of whiskey, or whatever else he can find, every day and he has done this for several years. The physical exam is notable for a hyperpigmented rash across his face, neck, chest, and the backs of his hands and forearms. On mental status exam, he is oriented to person and place but not time; he scores a 23/30 on the Montreal Cognitive Assessment (MOCA). This patient's presentation is most likely related to which of the following micronutrients?
A. Vitamin B2
B. Vitamin B12
C. Vitamin D
D. Vitamin C
E. Vitamin B3 (Correct Answer)
Explanation: ***Vitamin B3***
- The patient's symptoms—diarrhea, dermatitis (hyperpigmented rash), and dementia (disorientation to time, MOCA 23/30)—are the classic **3 Ds of pellagra**, which is caused by a **vitamin B3 (niacin) deficiency**.
- His chronic alcohol use and poor nutritional status (homelessness, recreational drug use) put him at high risk for such a deficiency, as alcohol impairs nutrient absorption and niacin is often lacking in the diets of those with limited food access.
*Vitamin B2*
- Deficiency in **vitamin B2 (riboflavin)** typically presents with cheilosis, angular stomatitis, glossitis, seborrheic dermatitis, and ocular symptoms like corneal vascularization, none of which are specifically mentioned here.
- While chronic alcohol use can also cause riboflavin deficiency, the patient's full symptom complex points more strongly to pellagra.
*Vitamin B12*
- **Vitamin B12 deficiency** often leads to **macrocytic anemia**, neurological symptoms including peripheral neuropathy, ataxia, and cognitive impairment, and glossitis, but it does not typically cause the characteristic dermatologic rash or diarrhea seen in this patient.
- While chronic alcohol use is a risk factor, the specific triad of diarrhea, dermatitis, and dementia is not consistent with B12 deficiency.
*Vitamin D*
- **Vitamin D deficiency** is associated with bone health issues (rickets in children, osteomalacia in adults), muscle weakness, and in severe cases, hypocalcemia.
- It does not present with the specific combination of diarrhea, hyperpigmented rash, and cognitive changes described in the patient.
*Vitamin C*
- **Vitamin C deficiency (scurvy)** typically manifests as perifollicular hyperkeratosis, bleeding gums, petechiae, impaired wound healing, and musculoskeletal pain.
- While malnourishment and alcohol abuse increase the risk of scurvy, the patient's symptoms do not align with the classic presentation of vitamin C deficiency.
Question 62: A 6-month-old boy is brought to the emergency department by his mother because of recurrent vomiting and yellowing of his eyes. The mother says that he has been eating poorly since she started weaning him off of breast milk 5 days ago. At this time, mashed vegetables and fruits were added to his diet. Examination shows scleral jaundice and dry mucous membranes. The tip of the liver is palpable 4 cm below the right costal margin. His serum glucose concentration is 47 mg/dL, serum alanine aminotransferase is 55 U/L, and serum aspartate aminotransferase is 66 U/L. Which of the following enzymes is most likely deficient?
A. Fructokinase
B. Glucose-6-phosphatase
C. Galactokinase
D. Galactose-1 phosphate uridyltransferase
E. Aldolase B (Correct Answer)
Explanation: ***Aldolase B***
- The symptoms, including **jaundice**, vomiting, **hepatomegaly**, and **hypoglycemia** following the introduction of solid foods (specifically fruits and vegetables containing **fructose**), are classic for **hereditary fructose intolerance**.
- **Aldolase B** is crucial for metabolizing fructose in the liver; its deficiency leads to the buildup of **fructose-1-phosphate**, which is toxic to hepatocytes and inhibits glucose production.
*Fructokinase*
- Fructokinase deficiency causes **essential fructosuria**, a benign condition characterized by fructose in the urine, but without the severe metabolic disturbances like hypoglycemia and liver damage seen in this patient.
- This condition does not typically present with the **jaundice**, vomiting, and liver enlargement found in the given case.
*Glucose-6-phosphatase*
- A deficiency in **glucose-6-phosphatase** causes **Type I glycogen storage disease (Von Gierke disease)**, which presents with severe hypoglycemia and hepatomegaly.
- However, it does not typically cause the **jaundice** or acute symptoms triggered by the introduction of solid foods containing fructose as described in this case.
*Galactokinase*
- Deficiency of galactokinase leads to **Type II galactosemia**, characterized primarily by **cataracts** and galactosemia, but typically without the profound liver damage, jaundice, or acute hypoglycemia seen here.
- The symptoms in this case are related to **fructose** intake, not galactose.
*Galactose-1 phosphate uridyltransferase*
- Deficiency in **galactose-1-phosphate uridyltransferase** causes **classic galactosemia**, which presents with **jaundice**, hepatosplenomegaly, vomiting, and cataracts, often triggered by lactose (galactose) intake.
- While it shares some symptoms with the patient's presentation, the trigger of symptoms upon introducing fruits and vegetables (high in fructose) points specifically to an issue with **fructose metabolism**, not galactose.
Question 63: A 2-year-old boy is brought to the emergency department by his mother 30 minutes after having a generalized tonic-clonic seizure. He was born at home and has not attended any well-child visits. He is not yet able to walk and does not use recognizable words. His paternal uncle has a severe intellectual disability and has been living in an assisted-living facility all of his life. The boy's urine phenylacetate level is markedly elevated. Which of the following amino acids is most likely nutritionally essential for this patient because of his underlying condition?
A. Alanine
B. Glutamate
C. Phenylalanine
D. Cysteine
E. Tyrosine (Correct Answer)
Explanation: ***Tyrosine***
- The patient's presentation with seizures, developmental delay, and elevated **phenylacetate (a phenylalanine metabolite)** strongly suggest **phenylketonuria (PKU)**.
- In PKU, the enzyme **phenylalanine hydroxylase (PAH)** is deficient, preventing the conversion of **phenylalanine** to **tyrosine**, making **tyrosine** a **nutritionally essential** amino acid.
*Alanine*
- **Alanine** is a **non-essential** amino acid synthesized from pyruvate and other amino acids, and its synthesis is not impaired in PKU.
- It plays a role in **gluconeogenesis** but is not directly related to the metabolic defect in PKU.
*Glutamate*
- **Glutamate** is a **non-essential** amino acid, crucial for neurotransmission and protein synthesis, and is not affected by PKU.
- It can be synthesized from various metabolic intermediates, and its status is not altered in patients with PKU.
*Phenylalanine*
- **Phenylalanine** is an **essential amino acid** that becomes **toxic** when accumulated due to PKU, making it necessary to restrict it in the diet.
- It is the precursor to **tyrosine**, but its inability to be metabolized is the core problem in PKU, not a nutritional essentiality related to the disease.
*Cysteine*
- **Cysteine** is a **conditionally essential** amino acid, often synthesized from methionine, and its synthesis is not directly impacted by PKU.
- While potentially essential in certain conditions, it is not the primary amino acid that becomes essential due to the specific enzymatic defect in PKU.
Question 64: A 4-month-old boy is brought to the physician because of a seizure. He was delivered at term after an uncomplicated pregnancy. He is currently at the 10th percentile for height, 5th percentile for weight, and 15th percentile for head circumference. Examination shows muscle hypotonia. His serum lactic acid and alanine are elevated. A functional assay of pyruvate dehydrogenase complex in serum leukocytes shows decreased enzyme activity. Supplementation with which of the following substances should be avoided in this patient?
A. Arachidonic acid
B. Riboflavin
C. Thiamine
D. Lysine
E. Valine (Correct Answer)
Explanation: ***Valine***
- While this is marked as the answer requiring avoidance, it's important to note that **branched-chain amino acids (BCAAs)** like valine, leucine, and isoleucine do NOT directly involve the pyruvate dehydrogenase complex in their metabolism.
- BCAAs are metabolized via **branched-chain α-keto acid dehydrogenase** (a separate enzyme complex) to produce acetyl-CoA and succinyl-CoA, **bypassing pyruvate dehydrogenase entirely**.
- In fact, ketogenic substrates that produce acetyl-CoA without generating pyruvate may be beneficial in PDC deficiency, as they provide energy without requiring PDC activity.
- **Note:** Among the listed options, none are classically contraindicated in PDC deficiency. The primary dietary modification in PDC deficiency is **carbohydrate restriction** (which produces pyruvate), not BCAA avoidance.
*Arachidonic acid*
- **Arachidonic acid** is an **omega-6 fatty acid** that serves as a precursor to eicosanoids and is important for normal development.
- Fatty acids are metabolized to acetyl-CoA via **β-oxidation**, which bypasses the pyruvate dehydrogenase complex entirely.
- High-fat, ketogenic diets are often **beneficial** in PDC deficiency, making fatty acid supplementation appropriate.
*Riboflavin*
- **Riboflavin (Vitamin B2)** is a precursor to **FAD and FMN**, coenzymes essential for the electron transport chain and various metabolic pathways.
- Riboflavin supplementation is sometimes beneficial in mitochondrial disorders and does not worsen PDC deficiency.
- It is considered safe and potentially therapeutic.
*Thiamine*
- **Thiamine (Vitamin B1)** is a crucial cofactor for **pyruvate dehydrogenase complex**, making it the most relevant therapeutic supplement for PDC deficiency.
- High-dose thiamine supplementation is often the **first-line treatment** in PDC deficiency, as it can enhance residual enzyme activity in some patients (particularly those with thiamine-responsive variants).
- Thiamine should be supplemented, not avoided.
*Lysine*
- **Lysine** is an essential amino acid that is exclusively **ketogenic**, being metabolized to **acetyl-CoA** without producing pyruvate.
- Since lysine metabolism bypasses PDC, it is safe and does not contribute to lactic acidosis.
- Lysine supplementation is not contraindicated in PDC deficiency.
Question 65: A 3-month-old boy is brought to the pediatrician by his mother after she notices orange sand–like crystalline material in her child’s diaper. He is not currently taking any medication and is exclusively breastfed. His immunizations are up to date. The doctor tells the mother that her son may have an X-linked recessive disorder. The boy is prescribed a medication that inhibits an enzyme responsible for the production of the crystals seen in his urine microscopy. Which of the following enzymes is the target of this medication?
A. Adenosine deaminase
B. Xanthine oxidase (Correct Answer)
C. Adenine phosphoribosyltransferase
D. Hypoxanthine-guanine phosphoribosyltransferase
E. Aminolevulinic acid synthetase
Explanation: ***Xanthine oxidase***
- The presence of **orange, sand-like crystalline material** in the diaper of a 3-month-old, along with the physician's comment about an **X-linked recessive disorder,** strongly suggests **Lesch-Nyhan syndrome**.
- In Lesch-Nyhan syndrome, a deficiency of **hypoxanthine-guanine phosphoribosyltransferase (HGPRT)** leads to an increase in **uric acid** production, which is then broken down by **xanthine oxidase**. Inhibiting xanthine oxidase with allopurinol is the treatment to reduce uric acid levels.
*Adenosine deaminase*
- Deficiency in **adenosine deaminase (ADA)** causes **severe combined immunodeficiency (SCID)** and would present with recurrent infections rather than crystalline urine.
- ADA is involved in purine metabolism, but its deficiency leads to the accumulation of deoxyadenosine and its phosphorylated derivatives, which are toxic to lymphocytes.
*Adenine phosphoribosyltransferase*
- Deficiency of **adenine phosphoribosyltransferase (APRT)** is associated with **2,8-dihydroxyadenine urolithiasis**, which can also cause renal stones, but it is much rarer than Lesch-Nyhan and typically presents differently (e.g., recurrent stone formation) rather than the classic "orange sand" in infants.
- This enzyme is involved in the salvage pathway of adenine.
*Hypoxanthine-guanine phosphoribosyltransferase*
- This enzyme, **HGPRT**, is the *deficient* enzyme in Lesch-Nyhan syndrome, not the enzyme targeted by medication.
- Its deficiency leads to the overproduction of uric acid precursors (hypoxanthine and guanine), which are then converted to uric acid by xanthine oxidase.
*Aminolevulinic acid synthetase*
- **Aminolevulinic acid synthetase (ALAS)** is involved in **heme synthesis**.
- Disorders related to this enzyme, such as **porphyrias**, would present with neurologic symptoms, psychiatric disturbances, or photosensitivity, not uric acid crystals in the urine.
Question 66: You have isolated cells from a patient with an unknown disorder and would like to locate the defect in this patient. When radiolabeled propionate is added to the mitochondria, no radiolabeled carbon dioxide is detected. However, when radiolabeled methylmalonic acid is added, radiolabeled carbon dioxide is detected from these cells. Which of the following amino acids can be fully metabolized by this patient?
A. Phenylalanine (Correct Answer)
B. Isoleucine
C. Methionine
D. Threonine
E. Valine
Explanation: ***Correct: Phenylalanine***
- This patient has a defect in **propionyl-CoA carboxylase**, which converts propionyl-CoA to methylmalonyl-CoA
- The inability to metabolize propionate but ability to process methylmalonic acid confirms the block is at propionyl-CoA carboxylase
- **Phenylalanine** is metabolized via the **phenylalanine hydroxylase pathway** to tyrosine, then to **fumarate** and **acetoacetate**
- This pathway does **not involve propionyl-CoA or methylmalonyl-CoA**, so phenylalanine can be fully metabolized
*Incorrect: Isoleucine*
- **Isoleucine** is a branched-chain amino acid that undergoes degradation to produce **propionyl-CoA**
- The defect in propionyl-CoA carboxylase would prevent conversion to methylmalonyl-CoA, blocking complete catabolism
- Propionyl-CoA would accumulate, preventing full metabolism
*Incorrect: Methionine*
- **Methionine** degradation produces **propionyl-CoA** through a minor pathway via α-ketobutyrate
- While the major pathway goes through homocysteine and transsulfuration to pyruvate, some methionine metabolism involves propionyl-CoA formation
- The propionyl-CoA carboxylase defect would impair complete catabolism
*Incorrect: Threonine*
- **Threonine** is metabolized by threonine dehydrogenase and can produce **propionyl-CoA** via α-ketobutyrate
- This requires propionyl-CoA carboxylase for complete oxidation to succinyl-CoA
- The enzymatic defect would prevent full breakdown
*Incorrect: Valine*
- **Valine** is a branched-chain amino acid that is degraded to **propionyl-CoA** via methylacrylyl-CoA
- Propionyl-CoA carboxylase deficiency would block further metabolism to methylmalonyl-CoA
- This would prevent complete oxidation to CO₂
Question 67: A 53-year-old homeless woman is brought to the emergency department by the police after she was found in the park lying unconscious on the ground. Both of her pupils are normal in size and reactive to light. There are no signs of head trauma. Finger prick test shows a blood glucose level of 20 mg/dL. She has been brought to the emergency department for acute alcohol intoxication several times before. Her vitals signs include: blood pressure 100/70 mm Hg, heart rate 90/min, respiratory rate 22/min, and temperature 35.0℃ (95.0℉). On general examination, she looks pale, but there is no sign of icterus noted. On physical examination, the abdomen is soft and non-tender and no hepatosplenomegaly noted. She spontaneously opens her eyes after the administration of a bolus of intravenous dextrose, thiamine, and naloxone. Blood and urine samples are drawn for toxicology screening. Finally, the blood alcohol level turns out to be 300 mg/dL. What will be the most likely laboratory findings in this patient?
A. Decreased MCV
B. AST > ALT, increased gamma-glutamyl transferase (Correct Answer)
C. Decreased ALP
D. ALT > AST, increased gamma-glutamyl transferase
E. AST > ALT, normal gamma-glutamyl transferase
Explanation: ***AST > ALT, increased gamma-glutamyl transferase***
- Chronic **alcohol abuse** typically leads to an elevation of **aspartate aminotransferase (AST)** that is greater than alanine aminotransferase (ALT), with an AST/ALT ratio commonly greater than 2:1.
- **Gamma-glutamyl transferase (GGT)** is a mitochondrial enzyme that is induced by alcohol, making its elevation a sensitive indicator of alcohol consumption and hepatotoxicity.
*AST > ALT, normal gamma-glutamyl transferase*
- While an AST/ALT ratio greater than 2:1 is consistent with alcoholic liver injury, a **normal GGT** would be highly unusual in a patient with chronic alcohol abuse and liver involvement, as GGT is notoriously sensitive to alcohol.
- A normal GGT would suggest a different etiology for the AST > ALT pattern, such as **muscle damage** or non-alcoholic steatohepatitis (NASH) in some cases, which is less likely here given the history.
*Decreased MCV*
- Chronic alcohol abuse more commonly leads to **macrocytosis** (increased MCV) due to direct toxic effects of alcohol on bone marrow and interference with folate metabolism, rather than decreased MCV.
- **Microcytosis** (decreased MCV) is typically indicative of iron deficiency anemia or thalassemia, which are not suggested by the patient's presentation.
*Decreased ALP*
- **Alkaline phosphatase (ALP)** is unlikely to be decreased in chronic alcohol abuse; it is more often **elevated** due to cholestasis or effects on bone.
- Decreased ALP can be seen in rare conditions like hypophosphatasia or severe malnutrition, but it is not a characteristic finding of alcoholic liver disease.
*ALT > AST, increase gamma glutamyl transferase*
- An **ALT > AST** ratio is more typical of non-alcoholic liver diseases such as viral hepatitis or non-alcoholic fatty liver disease (NAFLD).
- Although increased GGT is consistent with alcohol abuse, the **AST > ALT** pattern is the hallmark of alcoholic liver injury, contrasting with this option.
Question 68: A 25-year-old woman presents her physician with a complaint of feeling tired and low on energy for the past 6 months. She also has noticed she has been having trouble performing daily tasks and at times experiencing near-fainting spells. She has no recollection of similar instances in the past. Her past medical history is insignificant, except for the fact that she has been a strict vegan for the last 5 years. Her vital signs are stable. On physical examination, she is visibly pale and has decreased position and vibratory sensation in her both lower extremities. There is decreased lower limb reflexes with sensation intact. A complete blood count - done last week, - shows hemoglobin of 9.7 g/dL with an MCV of 110 fL. The serum levels of which of the following will most likely aid in the physician’s treatment plan?
A. Methylmalonic acid (Correct Answer)
B. Folate
C. Homocysteine
D. Succinyl CoA
E. Ferritin
Explanation: ***Methylmalonic acid***
- Elevated **methylmalonic acid (MMA)** levels, along with **macrocytic anemia (MCV 110 fL)** and neurological symptoms (decreased position and vibratory sensation, lower limb reflexes), are highly suggestive of **vitamin B12 deficiency**.
- As a strict **vegan**, the patient is at high risk for vitamin B12 deficiency because B12 is primarily found in animal products.
*Folate*
- While folate deficiency can cause **macrocytic anemia**, it typically does **not cause neurological symptoms** like those described.
- Furthermore, the neurological symptoms point more strongly towards vitamin B12 deficiency, which is crucial to differentiate from folate deficiency as folate supplementation alone can mask B12 deficiency and worsen neurological symptoms.
*Homocysteine*
- Elevated **homocysteine** can be seen in both **vitamin B12 and folate deficiencies**, making it less specific for differentiating between the two.
- Therefore, while it might be elevated, measuring MMA is more specific for confirming vitamin B12 deficiency.
*Succinyl CoA*
- **Succinyl CoA** is an intermediate in metabolism and is not directly measured to diagnose vitamin deficiencies.
- While its metabolism is affected by vitamin B12, measuring its precursor, **methylmalonic acid**, is the clinical diagnostic test.
*Ferritin*
- **Ferritin** levels are used to assess **iron stores** and diagnose iron deficiency anemia, which typically presents as **microcytic anemia**, not the **macrocytic anemia** seen in this patient (MCV 110 fL).
- Iron deficiency would not explain the neurological symptoms.
Question 69: A 25-year-old woman presents to the emergency department for the evaluation of a severe abdominal pain of 5 hours duration. The pain is colicky but is not localized. She also complains of nausea and an episode of vomiting. For the past 2 days, she has been constipated. She has had similar episodes of varying intensity in the past that resolved over a few hours. Several laboratory tests and imaging studies have been conducted in the past which were all within normal limits. The medical history is otherwise unremarkable. She denies smoking cigarettes or drinking alcohol. The vital signs are as follows: pulse 100/min, respiratory rate 16/min, and blood pressure 138/84 mm Hg. The physical examination reveals a young woman in obvious distress. There is no tenderness on abdominal examination. Laboratory tests are ordered, analgesics are administered, and the patient was admitted overnight for observation. In the morning, a urine sample was shown to have darkened overnight. Abnormal levels of which of the following most likely led to this patient’s condition?
A. Porphobilinogen deaminase (Correct Answer)
B. Coproporphyrinogen oxidase
C. Uroporphyrinogen decarboxylase
D. Uroporphyrinogen III synthase
E. Aminolevulinic acid dehydratase
Explanation: ***Porphobilinogen deaminase***
- This enzyme deficiency causes **acute intermittent porphyria (AIP)**, characterized by **acute neurovisceral attacks** with severe abdominal pain, nausea, vomiting, constipation, and neurological symptoms.
- The **darkening of urine overnight** is a classic sign of AIP, as excess **porphobilinogen** and **delta-aminolevulinic acid** in the urine oxidize upon standing.
*Coproporphyrinogen oxidase*
- Deficiency of this enzyme leads to **hereditary coproporphyria**, which presents with similar neurovisceral attacks to AIP, but it is less common.
- While it can also cause acute attacks and darkened urine, **AIP due to porphobilinogen deaminase deficiency** is the most common cause of acute porphyrias with neurovisceral symptoms and darkened urine.
*Uroporphyrinogen decarboxylase*
- Deficiency of this enzyme causes **porphyria cutanea tarda (PCT)**, the most common porphyria.
- PCT primarily manifests with **cutaneous symptoms** like photosensitivity, skin fragility, and blistering lesions, not acute abdominal pain or neurovisceral symptoms.
*Uroporphyrinogen III synthase*
- This enzyme deficiency causes **congenital erythropoietic porphyria (CEP)**, also known as Günther's disease.
- CEP is characterized by **severe photosensitivity**, **hemolysis**, and **erythrodontia (red teeth)**, with neurovisceral symptoms being uncommon.
*Aminolevulinic acid dehydratase*
- Deficiency of this enzyme causes **ALA dehydratase porphyria (ADP)**, a very rare form of porphyria.
- While it can manifest with neurovisceral symptoms, it is significantly **less common** than AIP.
Question 70: A 14-year-old boy is brought to the physician by his mother because of a 12-hour history of abdominal pain and dark urine. Three days ago, he developed a cough, sore throat, and rhinorrhea. Examination shows conjunctival pallor, scleral icterus, and mild splenomegaly. A peripheral blood smear shows small round inclusions within erythrocytes and several erythrocytes with semicircular indentations. The underlying cause of this patient's condition is most likely to also affect which of the following processes?
A. Anchoring proteins to cell surface
B. Function of myeloperoxidase
C. Biosynthesis of glutathione
D. Generation of superoxide (Correct Answer)
E. Conversion of phosphoenolpyruvate
Explanation: ***Generation of superoxide***
- This patient presents with signs of **hemolytic anemia** (abdominal pain, dark urine, conjunctival pallor, scleral icterus), likely triggered by an infection (cough, sore throat, rhinorrhea), and a peripheral blood smear showing **Heinz bodies** (small round inclusions) and **bite cells** (semicircular indentations). These findings are classic for **glucose-6-phosphate dehydrogenase (G6PD) deficiency**.
- **G6PD deficiency** impairs the **pentose phosphate pathway**, which is essential for producing **NADPH**. NADPH is required by **NADPH oxidase** for the **generation of superoxide** in phagocytes through the **respiratory burst** to kill bacteria.
*Anchoring proteins to cell surface*
- This process is primarily affected in diseases like **paroxysmal nocturnal hemoglobinuria** (PNH), where there is a defect in the **PIG-A gene** leading to deficient synthesis of **GPI anchors**.
- PNH presents with hemolytic anemia but lacks the characteristic Heinz bodies and bite cells seen in G6PD deficiency and is not typically triggered by infection in this acute manner.
*Function of myeloperoxidase*
- **Myeloperoxidase deficiency** leads to impaired killing of bacteria and fungi within phagocytes, increasing susceptibility to recurrent infections.
- While patients with myeloperoxidase deficiency have a normal respiratory burst, they do not present with hemolytic anemia or the specific red blood cell findings of G6PD deficiency.
*Conversion of phosphoenolpyruvate*
- **Pyruvate kinase deficiency** affects the final step in **glycolysis**, causing a buildup of **2,3-BPG** and impaired ATP production in red blood cells.
- This leads to chronic hemolytic anemia but does not present with Heinz bodies or bite cells, nor is it acutely triggered by infection in the same way as G6PD deficiency.
*Biosynthesis of glutathione*
- While G6PD deficiency impacts the **reduction of oxidized glutathione** (GSSG) back to **reduced glutathione** (GSH), it does not directly affect the *biosynthesis* of glutathione.
- The problem in G6PD deficiency is G6PD's inability to produce sufficient NADPH, which is a cofactor for **glutathione reductase**, thereby impairing the regeneration of GSH necessary to protect red blood cells from oxidative stress.