Question:medium

Regarding neurofibromatosis, all are true except:

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Is neurofibromatosis dominant or recessive?
Updated On: Jun 24, 2026
  • Autosomal recessive
  • Associated with cataract
  • Scoliosis
  • Multiple fibroma
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The Correct Option is A

Solution and Explanation

Step 1: The stem is a negative question, so the task is to find the single false claim among four. Three options should be established neurofibromatosis features and one should clash with its genetics.

Step 2: Neurofibromatosis is one of the well known autosomal dominant phakomatoses. The classic type one arises from a neurofibromin mutation on chromosome 17 and type two from a mutation on chromosome 22, and an affected parent can pass it on with each pregnancy.

Step 3: Cataract, scoliosis and crops of multiple neurofibromas all genuinely occur in the disease. Only the label autosomal recessive contradicts the dominant inheritance, so that statement is the exception being asked for.

\[\boxed{\text{Autosomal recessive is the false statement}}\]
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