WBR0437: Difference between revisions
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Rim Halaby (talk | contribs) Created page with "{{WBRQuestion |QuestionAuthor={{Rim}} |ExamType=USMLE Step 1 |MainCategory=Genetics |SubCategory=Neurology |MainCategory=Genetics |SubCategory=Neurology |MainCategory=Genetics..." |
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|MainCategory=Genetics | |MainCategory=Genetics | ||
|SubCategory=Neurology | |SubCategory=Neurology | ||
|Prompt=A 2 year old male | |Prompt=A 2-year-old male is brought by his mother to the physician’s office for seizures. The mother describes that the her son seems to have an “unusual” development as compared to his other siblings. Work-up of the patient reveals he has cortical and retinal hamartomas, renal angiomyolipoma, astrocytoma, and cardiac rhabdomyoma. Which of the following additional findings will most likely be present in this patient? | ||
|Explanation=[[Tuberous sclerosis]] is an [[autosomal dominant]] inherited disorder characterized by [[seizures]], [[mental retardation]], [[adenoma sebaceum]] on face, [[ash-leaf spots]] on skin, [[cortical]] and [[retinal]] [[hamartomas]], [[renal cysts]] and [[angiomyolipomas]], [[cardiac rhabdomyoma]], [[astrocytoma]]. The disease, however, has a variable presentation and an [[incomplete penetrance]]. | |Explanation=[[Tuberous sclerosis]] is an [[autosomal dominant]] inherited disorder characterized by [[seizures]], [[mental retardation]], [[adenoma sebaceum]] on face, [[ash-leaf spots]] on skin, [[cortical]] and [[retinal]] [[hamartomas]], [[renal cysts]] and [[angiomyolipomas]], [[cardiac rhabdomyoma]], [[astrocytoma]]. The disease, however, has a variable presentation and an [[incomplete penetrance]]. | ||