PubMed · 1971 · 64 citations · 0 references
MedicineDermatologyGeneticsEyelid DisordersHuman GeneticsOcular GeneticsCongenital Eye AnomaliesCongenital Skin DisordersKeratinization DisordersPigmentary DisordersPlantar Skin DisordersAutosomal Recessive InheritanceCongenital Keratinization DisordersCousin MarriageSyndromic Palmoplantar Keratoderma
Description is given of two sisters, offspring of a first cousin marriage, who exhibited the following identical lesions: 1) cysts of the borders of upper and lower lids; 2) hypodontia; 3) hypotrichosis; 4) palmo-plantar keratosis and 5) onychodystrophy. It is suggested that this combination represents a previously unrecognized autosomal recessive trait in man.