Diseases title

Hall-Riggs syndrome )

Dna2
Orpha Number: 2107
Synonym(s):

Hall-Riggs syndrome is a very rare syndrome consisting of microcephaly with facial dysmorphism, spondylometaepiphyseal dysplasia and severe intellectual deficit.Eight cases have been reported in the literature in two unrelated families.Dysmorphic features include hypertelorism, depressed nasal bridge, large nose with a large nasal tip, anteverted nostrils and wide mouth with thick lips. Affected patients do not achieve language ability.The condition is probably hereditary, and transmitted as an autosomal recessive trait.
source: Orphanet