Brachydactyly

A syndrome of high phenotypic variability caused by contiguous gene deletions in 2q37. The inheritance is autosomal dominant. The condition may be characterized by brachydactly type E; mental retardation; short stature; and other skeletal, cardiovascular, and neurologic manifestations.

Disease Alternative Name

brachydactyly mental retardation syndrome
chromosome 2q37 deletion syndrome
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Barpali
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MBBS and MD (pediatrics)

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Dr KUTE HOSPITAL

Dr KUTE HOSPITAL

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Kaithal (Haryana)
1502 followers
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