WBR0976: Difference between revisions
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|MainCategory=Biochemistry, Genetics | |MainCategory=Biochemistry, Genetics | ||
|SubCategory=General Principles | |SubCategory=General Principles | ||
|Prompt=A 28-year-old female is | |Prompt=A 28-year-old female is having a genetic counseling for metabolic disorders before her pregnancy. She is very worried that her future baby will carry the “bad gene” that her husband’s family has. Her husband’s brother has died when he was 7 due to coma resulting from an elevated level of ammonia in his blood. After reviewing the records, the lady is informed that her husband’s brother had the most common form of urea cycle disorder. What is the mode of inheritance of this disease? | ||
|Explanation=[[OTC|Ornithine transcarmylase]] (OTC) deficiency is the most common form of urea metabolism disorders. The [[urea cycle]] is composed of five enzymes, the deficiency in any of which might lead to a urea metabolism disorder. OTC deficiency is X-linked, whereas other urea metabolism disorders are autosomal recessive. | |Explanation=[[OTC|Ornithine transcarmylase]] (OTC) deficiency is the most common form of urea metabolism disorders. The [[urea cycle]] is composed of five enzymes, the deficiency in any of which might lead to a urea metabolism disorder. OTC deficiency is X-linked, whereas other urea metabolism disorders are autosomal recessive. Shown below is a diagram depicting the urea cycle. | ||
[[File:Urea Cycle Diagram.png|500px]] | |||
'''Educational objective:''' | '''Educational objective:''' |
Revision as of 21:22, 30 December 2013
Author | [[PageAuthor::Rim Halaby, M.D. [1]]] |
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Exam Type | ExamType::USMLE Step 1 |
Main Category | MainCategory::Biochemistry, MainCategory::Genetics |
Sub Category | SubCategory::General Principles |
Prompt | [[Prompt::A 28-year-old female is having a genetic counseling for metabolic disorders before her pregnancy. She is very worried that her future baby will carry the “bad gene” that her husband’s family has. Her husband’s brother has died when he was 7 due to coma resulting from an elevated level of ammonia in his blood. After reviewing the records, the lady is informed that her husband’s brother had the most common form of urea cycle disorder. What is the mode of inheritance of this disease?]] |
Answer A | AnswerA::Autosomal recessive |
Answer A Explanation | AnswerAExp::OTC deficiency is X-linked, whereas other urea metabolism disorders are autosomal recessive. |
Answer B | AnswerB::Autosomal dominant |
Answer B Explanation | AnswerBExp::OTC deficiency is X-linked, whereas other urea metabolism disorders are autosomal recessive. |
Answer C | AnswerC::X-linked recessive |
Answer C Explanation | AnswerCExp::OTC deficiency is X-linked, whereas other urea metabolism disorders are autosomal recessive. |
Answer D | AnswerD::X-linked dominant |
Answer D Explanation | AnswerDExp::OTC deficiency is X-linked, whereas other urea metabolism disorders are autosomal recessive. |
Answer E | AnswerE::Y-linked |
Answer E Explanation | AnswerEExp::OTC deficiency is X-linked, whereas other urea metabolism disorders are autosomal recessive. |
Right Answer | RightAnswer::C |
Explanation | [[Explanation::Ornithine transcarmylase (OTC) deficiency is the most common form of urea metabolism disorders. The urea cycle is composed of five enzymes, the deficiency in any of which might lead to a urea metabolism disorder. OTC deficiency is X-linked, whereas other urea metabolism disorders are autosomal recessive. Shown below is a diagram depicting the urea cycle.
Educational objective: OTC deficiency is X-linked, whereas other urea metabolism disorders are autosomal recessive. Reference:
First aid for USMLE step 1, 2013. Page 107. |
Approved | Approved::No |
Keyword | WBRKeyword::OTC, WBRKeyword::Urea cycle |
Linked Question | Linked:: |
Order in Linked Questions | LinkedOrder:: |