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|MainCategory=Biochemistry
|MainCategory=Biochemistry
|SubCategory=Neurology
|SubCategory=Neurology
|Prompt=A 1 year old boy is brought by his parents to the physician's office for failure to thrive. Upon further questioning, the mother explains that the child is aggressive, has abnormal movements, and is always chewing off his fingertips and lips. Physical examination is remarkable for swelling of the joints, spasticity, and hyperreflexia. Based on the illustration below, which enzyme is most likely deficient in this patient?
|Prompt=A one year old boy is brought by his parents to the physician's office for failure to thrive. Upon further questioning, the mother explains that the child is aggressive, has abnormal movements, and is always chewing off his fingertips and lips. Physical examination is remarkable for swelling of the joints, spasticity, and hyperreflexia. Based on the illustration below, which enzyme is most likely deficient in this patient?


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[[Image:WBR0320.png|500px]]
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|AnswerAExp="A" does not correspond to hypoxanthine-guanosine-phosphoribosyltransferase (HGPRT).
|AnswerAExp="A" does not correspond to hypoxanthine-guanosine-phosphoribosyltransferase (HGPRT).
|AnswerB=B
|AnswerB=B
|AnswerBExp="B" corresponds to HGPRT
|AnswerBExp="B" corresponds to HGPRT.
|AnswerC=C
|AnswerC=C
|AnswerCExp="C" does not correspond to HGPRT.
|AnswerCExp="C" does not correspond to HGPRT.

Revision as of 03:40, 19 November 2013

 
Author [[PageAuthor::Rim Halaby, M.D. [1]]]
Exam Type ExamType::USMLE Step 1
Main Category MainCategory::Biochemistry
Sub Category SubCategory::Neurology
Prompt [[Prompt::A one year old boy is brought by his parents to the physician's office for failure to thrive. Upon further questioning, the mother explains that the child is aggressive, has abnormal movements, and is always chewing off his fingertips and lips. Physical examination is remarkable for swelling of the joints, spasticity, and hyperreflexia. Based on the illustration below, which enzyme is most likely deficient in this patient?

]]

Answer A AnswerA::A
Answer A Explanation AnswerAExp::"A" does not correspond to hypoxanthine-guanosine-phosphoribosyltransferase (HGPRT).
Answer B AnswerB::B
Answer B Explanation AnswerBExp::"B" corresponds to HGPRT.
Answer C AnswerC::C
Answer C Explanation AnswerCExp::"C" does not correspond to HGPRT.
Answer D AnswerD::D
Answer D Explanation AnswerDExp::"D" does not correspond to HGPRT. It corresponds to adenosine deaminase (ADA). Its absence causes severe combined immunodeficiency (SCID).
Answer E AnswerE::E
Answer E Explanation AnswerEExp::"E" does not correspond to HGPRT.
Right Answer RightAnswer::B
Explanation [[Explanation::The patient has symptoms and signs consistent with Lesch-Nyhan syndrome, an X-linked disorder characterized by the absence of hypoxanthine-ribosyl-phosphoribosyltransferase (HGPRT), which normally converts hypoxanthine to inosinic acid (IMP) and guanine to guanylic acid (GMP). As a result, the purine salve pathway is lost and the patient has to undergo de novo purine synthesis. Excessive uric acid production in urea and increase in purine synthesis enzymes, along with the absence of any HGPRT activity and hyperuricemia, are present. Patients typically present with mental retardation, failure to thrive, choreoathetosis, and self-aggressive behavior with self-mutilation. Joint swelling is due to gout due to hyperuricemia.

Educational Objective: Absence of HGPRT causes Lesch-Nyhan syndrome, characterized by mental retardation, self-mutilation, hyperuricemia, and choreoathetosis.
Educational Objective:
References: ]]

Approved Approved::No
Keyword WBRKeyword::HGPRT, WBRKeyword::lesch, WBRKeyword::nyhan, WBRKeyword::syndrome, WBRKeyword::self-mutilation, WBRKeyword::self, WBRKeyword::mutilation, WBRKeyword::aggressive, WBRKeyword::behavior, WBRKeyword::aggression, WBRKeyword::hyperuricemia, WBRKeyword::gout, WBRKeyword::hypoxanthine, WBRKeyword::guanine, WBRKeyword::phosphoribosyltransferase, WBRKeyword::purine, WBRKeyword::salvage, WBRKeyword::de, WBRKeyword::novo, WBRKeyword::X-linked, WBRKeyword::congenital, WBRKeyword::disorder
Linked Question Linked::
Order in Linked Questions LinkedOrder::