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{{WBRQuestion | {{WBRQuestion | ||
|QuestionAuthor=William J Gibson | |QuestionAuthor=William J Gibson (Reviewed by {{YD}}) | ||
|ExamType=USMLE Step 1 | |ExamType=USMLE Step 1 | ||
|MainCategory=Biochemistry, Genetics | |MainCategory=Biochemistry, Genetics | ||
Line 21: | Line 21: | ||
|MainCategory=Biochemistry, Genetics | |MainCategory=Biochemistry, Genetics | ||
|SubCategory=Hematology | |SubCategory=Hematology | ||
|Prompt=A newborn | |Prompt=A newborn boy is born to a gravida 1 para 1 33-year-old woman by normal vaginal delivery. The woman received proper prenatal care including folic acid supplementation. The child undergoes circumcision, but his bleeding does not cease for 4 hours. The physician orders laboratory testing which reveals: Increased PTT, normal PT, and platelets of 235,000. Further evaluation demonstrates Factor VIII activity 4% of normal. What is the mode of inheritance of the most likely condition? | ||
|Explanation=The patient in this vignette has Hemophilia A, an X-linked recessive bleeding disorder caused by a deficiency of Factor VIII. Factor VIII normally functions to promote the function of the intrinsic coagulation cascade and cause fibrin cross-linked clots to form. One of the earliest signs of hemophilia can be abnormally long bleeding following circumcision. In both Hemophilia A and B, spontaneous bleeding is common. On laboratory testing, these patients have a normal bleeding time, normal prothrombin time, normal thrombin time, but prolonged partial thromboplastin time. The most characteristic type of internal bleed is a joint bleed where blood enters into the joint spaces. Bleeding can be controlled with regular infusions of the deficient clotting factor, i.e. factor VIII in Hemophilia A or factor IX in Hemophilia B. | |Explanation=The patient in this vignette has Hemophilia A, an X-linked recessive bleeding disorder caused by a deficiency of Factor VIII. Factor VIII normally functions to promote the function of the intrinsic coagulation cascade and cause fibrin cross-linked clots to form. One of the earliest signs of hemophilia can be abnormally long bleeding following circumcision. In both Hemophilia A and B, spontaneous bleeding is common. On laboratory testing, these patients have a normal bleeding time, normal prothrombin time, normal thrombin time, but prolonged partial thromboplastin time. The most characteristic type of internal bleed is a joint bleed where blood enters into the joint spaces. Bleeding can be controlled with regular infusions of the deficient clotting factor, i.e. factor VIII in Hemophilia A or factor IX in Hemophilia B. | ||
|AnswerA=Autosomal recessive | |AnswerA=Autosomal recessive |
Revision as of 17:55, 10 November 2014
Author | [[PageAuthor::William J Gibson (Reviewed by Yazan Daaboul, M.D.)]] |
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Exam Type | ExamType::USMLE Step 1 |
Main Category | MainCategory::Biochemistry, MainCategory::Genetics |
Sub Category | SubCategory::Hematology |
Prompt | [[Prompt::A newborn boy is born to a gravida 1 para 1 33-year-old woman by normal vaginal delivery. The woman received proper prenatal care including folic acid supplementation. The child undergoes circumcision, but his bleeding does not cease for 4 hours. The physician orders laboratory testing which reveals: Increased PTT, normal PT, and platelets of 235,000. Further evaluation demonstrates Factor VIII activity 4% of normal. What is the mode of inheritance of the most likely condition?]] |
Answer A | AnswerA::Autosomal recessive |
Answer A Explanation | AnswerAExp::Hemophilia A is not an autosomal recessive disorder. An example of an autosomal recessive disease is phenylketonuria. |
Answer B | AnswerB::Autosomal dominant |
Answer B Explanation | AnswerBExp::Hemophilia A is not an autosomal dominant disorder. An example of an autosomal dominant disorder is von Willebrand disease. |
Answer C | AnswerC::X-linked dominant |
Answer C Explanation | AnswerCExp::Hemophilia is not an X-linked dominant disorder. An example of an X-linked dominant disorder is Rett syndrome. |
Answer D | AnswerD::X-linked recessive |
Answer D Explanation | AnswerDExp::One of the first sign of Hemophilia can be abnormally prolonged bleeding following circumcision. Hemophilia A is an X-linked recessive disorder. |
Answer E | AnswerE::Mitochondrial |
Answer E Explanation | AnswerEExp::Hemophilia A is not a mitochondrial disorder. An example of a mitochondrial disorder is Leber’s hereditary optic neuropathy. |
Right Answer | RightAnswer::D |
Explanation | [[Explanation::The patient in this vignette has Hemophilia A, an X-linked recessive bleeding disorder caused by a deficiency of Factor VIII. Factor VIII normally functions to promote the function of the intrinsic coagulation cascade and cause fibrin cross-linked clots to form. One of the earliest signs of hemophilia can be abnormally long bleeding following circumcision. In both Hemophilia A and B, spontaneous bleeding is common. On laboratory testing, these patients have a normal bleeding time, normal prothrombin time, normal thrombin time, but prolonged partial thromboplastin time. The most characteristic type of internal bleed is a joint bleed where blood enters into the joint spaces. Bleeding can be controlled with regular infusions of the deficient clotting factor, i.e. factor VIII in Hemophilia A or factor IX in Hemophilia B. Educational Objective: Hemophilia A is an X-linked recessive disease. |
Approved | Approved::Yes |
Keyword | WBRKeyword::Blood, WBRKeyword::Bleeding, WBRKeyword::Circumcision, WBRKeyword::Hemophilia, WBRKeyword::X-linked, WBRKeyword::X-linked recessive, WBRKeyword::Coagulation |
Linked Question | Linked:: |
Order in Linked Questions | LinkedOrder:: |