Erythrokeratoderma variabilis: a case report
نویسندگان
چکیده
منابع مشابه
Erythrokeratoderma variabilis without connexin 31 or connexin 30.3 gene mutation: immunohistological, ultrastructural and genetic studies.
Erythrokeratoderma variabilis, characterized by migrating erythema and fixed keratotic plaques, is a rare congenital disorder which has recently been connected with connexin (Cx)30.3 or Cx31 gene mutations. We present a 9-month-old Japanese girl who exhibited the typical clinical features of the disease, but carried no Cx30.3 or Cx31 gene mutations. Histopathologically, regular acanthosis with ...
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ژورنال
عنوان ژورنال: International Journal of Research in Dermatology
سال: 2021
ISSN: 2455-4529
DOI: 10.18203/issn.2455-4529.intjresdermatol20212558