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Figure 1 | BMC Medical Genetics

Figure 1

From: Heterozygous p.Asp50Asn mutation in the GJB2 gene in two Cameroonian patients with keratitis-ichthyosis-deafness (KID) syndrome

Figure 1

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.

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BMC Medical Genetics

ISSN: 1471-2350

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