Vohwinkel syndrome

Genetics

• autosomal dominant
• associated with defects in connexin-26 (GJB2)

Clinical manifestations

• hyperkeratosis
• constriction on finger & toes
• congenital deafness

More general terms

• genetic syndrome (multisystem disorder)

More specific terms

• Vohwinkel syndrome with ichthyosis; Loricrin keratoderma; mutilating keratoderma with ichthyosis

Database

• OMIM: https://mirror.omim.org/entry/124500