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|AnswerEExp=Cystic medial necrosis of the aorta is frequently observed in patients with [[Marfan syndrome]], a mutation of the FBN1 gene that encodes fibrillin.  
|AnswerEExp=Cystic medial necrosis of the aorta is frequently observed in patients with [[Marfan syndrome]], a mutation of the FBN1 gene that encodes fibrillin.  
|RightAnswer=A
|RightAnswer=A
|WBRKeyword=tuberous sclerosis, ash leaf spot, hamartoma, angiomyolipoma, rhabdomyoma, astrocytoma, autosomal dominant, inheritance, genetics, expression
|WBRKeyword=tuberous sclerosis, hamartoma, angiomyolipoma, rhabdomyoma, astrocytoma, autosomal dominant, inheritance, genetics, expression
|Approved=Yes
|Approved=Yes
}}
}}

Revision as of 18:48, 22 July 2014

 
Author [[PageAuthor::Rim Halaby, M.D. [1], Alison Leibowitz [2] (Reviewed by Alison Leibowitz)]]
Exam Type ExamType::USMLE Step 1
Main Category MainCategory::Genetics
Sub Category SubCategory::Neurology
Prompt [[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 has been developing unusually when compared to his siblings. Work-up reveals cortical and retinal hamartomas, renal angiomyolipoma, astrocytoma, and cardiac rhabdomyoma. Which of the following additional findings will most likely be present in this patient?]]
Answer A AnswerA::Fitzpatrick patches (Ash-leaf spots)
Answer A Explanation AnswerAExp::See explanation.
Answer B AnswerB::Oral ganglioneuromas
Answer B Explanation AnswerBExp::Oral neurogangliomas are frequently observed in MEN2B syndrome, which results from a mutation of the ret oncogene.
Answer C AnswerC::Retinal hemangioblastoma
Answer C Explanation [[AnswerCExp::Renal hemangioblastoma is frequently observed in von Hippel-Lindau disease, which results from a deletion of the VHL gene on chromosome 3.]]
Answer D AnswerD::Bilateral acoustic schwannomas
Answer D Explanation [[AnswerDExp::Bilateral acoustic schwannomas are frequently observed in neurofibromatosis type II. The NF2 gene is located on chromosome 22.]]
Answer E AnswerE::Cystic medial necrosis of the aorta
Answer E Explanation [[AnswerEExp::Cystic medial necrosis of the aorta is frequently observed in patients with Marfan syndrome, a mutation of the FBN1 gene that encodes fibrillin.]]
Right Answer RightAnswer::A
Explanation [[Explanation::Tuberous sclerosis is an autosomal dominant inherited disorder frequently characterized by seizures, mental retardation, facial adenoma sebaceum, ash-leaf spots on skin, cortical and retinal hamartomas, renal cysts, angiomyolipomas, cardiac rhabdomyoma, and astrocytoma. The disease has a variable presentation and incomplete penetrance.

Educational Objective: Tuberous sclerosis is an autosomal dominant inherited disorder frequently characterized by seizures, mental retardation, facial adenoma sebaceum, ash-leaf spots on skin, cortical and retinal hamartomas, renal cysts, angiomyolipomas, cardiac rhabdomyoma, and astrocytoma.
References: First Aid 2014 page 87]]

Approved Approved::Yes
Keyword WBRKeyword::tuberous sclerosis, WBRKeyword::hamartoma, WBRKeyword::angiomyolipoma, WBRKeyword::rhabdomyoma, WBRKeyword::astrocytoma, WBRKeyword::autosomal dominant, WBRKeyword::inheritance, WBRKeyword::genetics, WBRKeyword::expression
Linked Question Linked::
Order in Linked Questions LinkedOrder::