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Vohwinkel syndrome
Genetics:
- autosomal dominant
- associated with defects in connexin-26 (GJB2)
Clinical manifestations:
- hyperkeratosis
- constriction on finger & toes
- congenital deafness
Specific
Vohwinkel syndrome with ichthyosis; Loricrin keratoderma; mutilating keratoderma with ichthyosis
General
genetic syndrome (multisystem disorder)
Database Correlations
OMIM 124500
References
OMIM :accession 124500