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?
ASphingomyelinase deficiency
Bβ-glucocerebrosidase deficiency
Cα-galactosidase A deficiency
DATP-binding cassette transporter mutation
Eβ-hexosaminidase A deficiency
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?
ACeramide trihexoside
BCerebroside sulfate
CGlucocerebroside
DSphingomyelin
ELimit dextrin
A 2-year-old boy is brought to the emergency department by his parents because of fever and recurrent episodes of jerky movements of his extremities for the past 6 hours. Pregnancy and delivery were uncomplicated, and development was normal until the age of 1 year. The parents report that he has had gradual loss of speech, vision, and motor skills over the past year. During this time, he has been admitted to the hospital three times because of myoclonic seizures. Physical examination shows hypertonicity of the upper and lower extremities. Fundoscopic examination shows pallor of the optic disc bilaterally. An MRI of the brain shows brain atrophy and hyperintensity of the periventricular and subcortical areas. Two days after admission, the patient dies. Histopathologic examination of the brain shows aggregation of globoid cells and loss of glial cells. The patient’s condition was most likely caused by a deficiency of which of the following enzymes?
Aβ-Galactocerebrosidase
Bβ-Glucocerebrosidase
CArylsulfatase A
DSphingomyelinase
Eβ-Hexosaminidase A
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