WBR0255: Difference between revisions
Jump to navigation
Jump to search
Created page with "{{WBRQuestion |QuestionAuthor=William J Gibson |ExamType=USMLE Step 1 |MainCategory=Biochemistry, Genetics |SubCategory=Hematology |MainCategory=Biochemistry, Genetics |SubCat..." |
No edit summary |
||
Line 8: | Line 8: | ||
|MainCategory=Biochemistry, Genetics | |MainCategory=Biochemistry, Genetics | ||
|SubCategory=Hematology | |SubCategory=Hematology | ||
|MainCategory=Biochemistry, Genetics | |||
|MainCategory=Biochemistry, Genetics | |MainCategory=Biochemistry, Genetics | ||
|MainCategory=Biochemistry, Genetics | |MainCategory=Biochemistry, Genetics | ||
Line 21: | Line 22: | ||
|SubCategory=Hematology | |SubCategory=Hematology | ||
|Prompt=A newborn male 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? | |Prompt=A newborn male 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 | ||
|AnswerAExp= | |AnswerAExp=Hemophilia A is not an autosomal recessive disorder. An example of an autosomal recessive disease is phenylketonuria. | ||
|AnswerB=Autosomal dominant | |AnswerB=Autosomal dominant | ||
|AnswerBExp= | |AnswerBExp=Hemophilia A is not an autosomal dominant disorder. An example of an autosomal dominant disorder is von Willebrand disease. | ||
|AnswerC=X-linked dominant | |AnswerC=X-linked dominant | ||
|AnswerCExp= | |AnswerCExp=Hemophilia is not an X-linked dominant disorder. An example of an X-linked dominant disorder is Rett syndrome. | ||
|AnswerD=X-linked recessive | |AnswerD=X-linked recessive | ||
|AnswerDExp= | |AnswerDExp=One of the first sign of Hemophilia can be abnormally prolonged bleeding following circumcision. Hemophilia A is an X-linked recessive disorder. | ||
|AnswerE=Mitochondrial | |AnswerE=Mitochondrial | ||
|AnswerEExp= | |AnswerEExp=Hemophilia A is not a mitochondrial disorder. An example of a mitochondrial disorder is Leber’s hereditary optic neuropathy. | ||
|EducationalObjectives=Hemophilia A is an X-linked recessive disease. | |||
|References=First Aid 2012 page 389 | |||
|RightAnswer=D | |RightAnswer=D | ||
|WBRKeyword=Blood, Bleeding, Circumcision, Hemophilia, X-linked, X-linked recessive, Coagulation, | |WBRKeyword=Blood, Bleeding, Circumcision, Hemophilia, X-linked, X-linked recessive, Coagulation, | ||
|Approved=Yes | |Approved=Yes | ||
}} | }} |
Revision as of 03:24, 11 September 2014
Author | PageAuthor::William J Gibson |
---|---|
Exam Type | ExamType::USMLE Step 1 |
Main Category | MainCategory::Biochemistry, MainCategory::Genetics |
Sub Category | SubCategory::Hematology |
Prompt | [[Prompt::A newborn male 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:: |