WBR0976: Difference between revisions

Jump to navigation Jump to search
(Created page with "{{WBRQuestion |QuestionAuthor={{Rim}} |ExamType=USMLE Step 1 |MainCategory=Biochemistry, Genetics |SubCategory=General Principles |MainCategory=Biochemistry, Genetics |SubCate...")
 
No edit summary
Line 20: Line 20:
|MainCategory=Biochemistry, Genetics
|MainCategory=Biochemistry, Genetics
|SubCategory=General Principles
|SubCategory=General Principles
|Prompt=A 28-year-old female is being counseled 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 nephews had the most common form of urea cycle disorder.  What is the mode of inheritance of this disease?
|Prompt=A 28-year-old female is counseled 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.
'''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.
|AnswerA=Autosomal recessive
|AnswerA=Autosomal recessive
|AnswerAExp=OTC deficiency is X-linked, whereas other urea metabolism disorders are autosomal recessive.
|AnswerAExp=OTC deficiency is X-linked, whereas other urea metabolism disorders are autosomal recessive.
Line 33: Line 39:
|AnswerEExp=OTC deficiency is X-linked, whereas other urea metabolism disorders are autosomal recessive.
|AnswerEExp=OTC deficiency is X-linked, whereas other urea metabolism disorders are autosomal recessive.
|RightAnswer=C
|RightAnswer=C
|WBRKeyword=OTC, Urea cycle,  
|WBRKeyword=OTC, Urea cycle,
|Approved=No
|Approved=No
}}
}}

Revision as of 23:59, 29 December 2013

 
Author [[PageAuthor::Rim Halaby, M.D. [1]]]
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 counseled 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.

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.
Educational Objective:
References: ]]

Approved Approved::No
Keyword WBRKeyword::OTC, WBRKeyword::Urea cycle
Linked Question Linked::
Order in Linked Questions LinkedOrder::