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odontoonychodermal dysplasia
Epidemiology: rare
Pathology: ectodermal dysplasia
Genetics:
- autosomal recessive
- associated with defects in WNT10A
Clinical manifestations:
- presenting phenotype is dry hair, severe hypodontia, smooth tongue with marked reduction of fungiform & filiform papillae, onychodysplasia, keratoderma & hyperhidrosis of palms & soles, & hyperkeratosis of the skin
General
genetic syndrome (multisystem disorder)
Database Correlations
OMIM 257980
References
OMIM :accession 257980