Acrodermatitis enteropathica: a hereditary form of zinc deficiency

Author:

Higuchi S1ORCID,Yorifuji T1,Nishida M2,Fukai K2,Nakano H3

Affiliation:

1. Division of Pediatric Endocrinology and Metabolism, Children’s Medical Center, Osaka City General Hospital, 2-13-22, Miyakojima-Hondori, Miyakojima, Osaka 534-0021, Japan

2. Department of Dermatology, Osaka City General Hospital, 2-13-22, Miyakojima-Hondori, Miyakojima, Osaka 534-0021, Japan

3. Department of Dermatology, Hirosaki University Graduate School of Medicine, 5, Zaifu-cho, Hirosaki-city, Aomori 036-8562, Japan

Publisher

Oxford University Press (OUP)

Subject

General Medicine

Reference4 articles.

1. Acrodermatitis enteropathica: an uncommon differential diagnosis in childhood – first description of a new sequence variant;Jung;J Dtsch Dermatol Ges,2011

2. Novel and recurrent nonsense mutation of the SLC39A4 gene in Japanese patients with acrodermatitis enteropathica;Nakano;Br J Dermatol,2009

3. Identification of SLC39A4, a gene involved in acrodermatitis enteropathica;Küry;Nat Genet,2002

4. Transient symptomatic zinc deficiency in a breast-fed infant: relevance of a genetic study;El Fékih;Nutrition,2011

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