Figure 1From: Heterozygous p.Asp50Asn mutation in the GJB2 gene in two Cameroonian patients with keratitis-ichthyosis-deafness (KID) syndrome Illustrations of some clinical features of the two Cameroonian KID cases (Case 1; panels A-D; Case 2 panels E and F). A) Keratoderma of the soles B) Rippled hyperkeratotic plaques on the knees; C) Hypotrichosis of the eyelashes and eyebrows; D) Mild vascularizing keratitis; E) Hyperkeratosis of the hands; F) Alopecia, hypotrichosis, ichthyosiform erythrokeratoderma.Back to article page