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Up to: Autosomal dominant disease · Multiple congenital anomalies/dysmorphic syndrome-intellectual disability · Partial deletion of the long arm of chromosome 8 · Trichorhinophalangeal syndrome
Trichorhinophalangeal syndrome type II
Langer-Giedon syndrome, also known as trichorhinophalangeal syndrome type 2, is a very rare, genetic, multiple congenital anomaly disorder characterized by bone abnormalities, distinctive facial features, multiple exostoses, and intellectual disability.
This condition has no sub-types.