Can ya help me with this Step 1 question?

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neuroace

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A 5-year-old boy is brought to the physician by his parents because of an 8-month history of difficulty walking. His parents say that he limps when he walks and has a waddling gait; he also has difficulty standing. When getting up from a sitting position, he uses his hands to walk up his thighs and push his body into a standing position. His mother is an only child but she has an uncle who became bedridden as a child and died of respiratory arrest. Physical examination of the boy shows prominent calf muscles.


Which corresponding gene is likely to be the cause of the boy’s condition.


A. Fibrillin 1

B. Dystrophin

C. Acid α glucosidase

D. Myotonin kinase

E. Frataxin


Friend and I disagree upon answer. I thought B. As in Duchenne muscular dystrophy.
 
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You are correct, he exhibits gowers sign and has pseudohypertrophy of his calves, as well as a family history that sounds like it is x linked recessive. Dystrophin is the answer .

yeah i agree, and he is also showing gower's sign which is using your hand to get up to due weakness in the proximal muscle so yes i agree!
 
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