
doi: 10.1159/000251645
pmid: 4212018
The case of an 11-year-old girl with typical symptoms of focal dermal hypoplasia (Goltz-Gorlin syndrome) is reported. In a mentally normal child a mild body asymmetry with ocular, skin, dental, and skeletal changes, more pronounced on the right side, has been detected. A special contribution to the presentation is the dermatoglyphic finding of epidermal ridge hypoplasia on the fingertips of the right hand.
Leg, Tooth Abnormalities, Syndrome, Toes, Skin Diseases, Fingers, Humans, Abnormalities, Multiple, Female, Eye Abnormalities, Telangiectasis, Atrophy, Dermatoglyphics, Child, Pigmentation Disorders, Skin
Leg, Tooth Abnormalities, Syndrome, Toes, Skin Diseases, Fingers, Humans, Abnormalities, Multiple, Female, Eye Abnormalities, Telangiectasis, Atrophy, Dermatoglyphics, Child, Pigmentation Disorders, Skin
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