tricho-rhino-phalangeal syndrome type 2
tricho-rhino-phalangeal syndrome type 2
A hereditary condition (OMIM:150230) with features of both tricho-rhino-phalangeal syndrome type 1 and multiple exostoses type 1, and which is characterised by multiple dysmorphic facial features (e.g., large, laterally protruding ears, a bulbous nose, an elongated upper lip and sparse scalp hair), winged scapulae, multiple cartilaginous exostoses, redundant skin and mental retardation.Molecular pathology
Defects of TRPS1 and EXT1 are present in tricho-rhino-phalangeal syndrome type 2.