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Review Question - QID 5877

Achondroplasia Etiology Genetics QID: 5877 (OBQ15.192)
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QID 5877 (Type "5877" in App Search)
A 12-year-old male has an autosomal dominant genetic condition caused by a mutation on chromosome 4p. The mutation causes increased tyrosine kinase activity in the proliferative zone during enchondral bone formation at the physis. This condition is known as:
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