WBR0219
Author | [[PageAuthor::William J Gibson (Reviewed by Yazan Daaboul, M.D.)]] |
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Exam Type | ExamType::USMLE Step 1 |
Main Category | MainCategory::Genetics, MainCategory::Pathophysiology |
Sub Category | SubCategory::Head and Neck, SubCategory::Renal |
Prompt | [[Prompt::A 7-year-old boy is brought to his primary care physician for progressive bilateral deafness. Family history is significant for multiple family members who suffered from a similar condition at childhood. Physical examination is remarkable for subcapsular posterior lens opacities and sensorineural deafness. The physician suspects the patient's condition is caused by a genetic disease. Genetic testing results demonstrate a frameshift mutation in the COL4A5 gene. Further work-up will most likely be remarkable for abnormalities in which of the following tests?]] |
Answer A | AnswerA::Serum creatinine |
Answer A Explanation | [[AnswerAExp::Alport's syndrome is a familial cause of deafness, ocular disturbances, and nephritis. Although patients eventually develop end stage renal disease (ESRD), serum creatinine is often normal early in the course of the disease, and the diagnosis may be missed.]] |
Answer B | AnswerB::Electrocardiogram |
Answer B Explanation | AnswerBExp::Alport's syndrome is not primarily associated with cardiac disease or changes on electrocardiogram (ECG). |
Answer C | AnswerC::Urinalysis |
Answer C Explanation | [[AnswerCExp::Alport's syndrome is a familial cause of deafness, ocular disturbances, and nephritis. Microscopic hematuria is the most common presenting sign of patients with Alport's syndrome. Hematuria is usually present before patients experience symptoms of renal failure (eg. hypertension) and before an elevation in serum creatinine is observed.]] |
Answer D | AnswerD::Alanine aminotransferase |
Answer D Explanation | AnswerDExp::Alport syndrome is not primarily associated with abnormal values of alanine aminotransferase (ALT) or liver abnormalities. |
Answer E | AnswerE::Platelet counts |
Answer E Explanation | AnswerEExp::Alport's syndrome is not primarily associated with quantitative platelet disturbances. |
Right Answer | RightAnswer::C |
Explanation | [[Explanation::{ Educational Objective: Alport's syndrome is a familial cause of deafness, ocular disturbances, and nephritis. |
Approved | Approved::Yes |
Keyword | WBRKeyword::Alport's syndrome, WBRKeyword::Alport, WBRKeyword::Nephritis, WBRKeyword::Deafness, WBRKeyword::Hearing loss, WBRKeyword::Hematuria, WBRKeyword::Creatinine, WBRKeyword::Work-up, WBRKeyword::COL4A5, WBRKeyword::Hereditary nephritis |
Linked Question | Linked:: |
Order in Linked Questions | LinkedOrder:: |