Browsing by Author "Durmaz, C. D."
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H syndrome: a genodermatosis characterised by hyperpigmented, and hypertrichotic skin
An, I; Durmaz, C. D.; Ruhi, H., I; Ertop, P.; Ozturk, M.; Sula, B.; Ecer, N. (Medcom Ltd, 2019)H syndrome is an autosomal recessive genodermatosis caused by SLC29A3 gene mutation. An important feature of the H syndrome is the hyperpigmented patchs and plaques, usually accompanied by hypertrichosis, seen in the inner ...