Under-recognition of acral peeling skin syndrome: 59 new cases with 15 novel mutations.

Szczecinska, W; Nesteruk, D; Wertheim-Tysarowska, K; Greenblatt, D T; Baty, D; Browne, F; Liu, L; Ozoemena, L; Terron-Kwiatkowski, A; McGrath, J A; Mellerio, J E; Morton, J; Wozniak, K; Kowalewski, C; Has, C; Moss, C

Szczecinska, W; Nesteruk, D; Wertheim-Tysarowska, K; Greenblatt, D T; Baty, D; Browne, F; Liu, L; Ozoemena, L; Terron-Kwiatkowski, A; McGrath, J A; Mellerio, J E; Morton, J; Wozniak, K; Kowalewski, C; Has, C; Moss, C.

Affiliation

Szczecinska W; Department of Dermatology, Birmingham Children's Hospital, Steelhouse Lane, Birmingham, B4 6NH, U.K.

Br J Dermatol ; 171(5): 1206-10, 2014 Nov.

Article in En | MEDLINE | ID: mdl-24628291

Subject(s)

Dermatitis, Exfoliative/genetics; Mutation/genetics; Pigmentation Disorders/genetics; Transglutaminases/genetics; Child; Dermatitis, Exfoliative/diagnosis; Dermatitis, Exfoliative/ethnology; Diagnosis, Differential; Epidermolysis Bullosa Simplex/diagnosis; Founder Effect; Genetic Testing; Germany/ethnology; Heterozygote; Homozygote; Humans; Keratin-14/genetics; Keratin-5/genetics; Pigmentation Disorders/diagnosis; Pigmentation Disorders/ethnology; Poland/ethnology; Skin Diseases/congenital; United Kingdom/ethnology

Fulltext

XML

PubMed Links

Search on Google

Full text: 1 Database: MEDLINE Main subject: Pigmentation Disorders / Transglutaminases / Dermatitis, Exfoliative / Mutation Type of study: Diagnostic_studies / Prognostic_studies Limits: Child / Humans Country/Region as subject: Europa Language: En Year: 2014 Type: Article

Fulltext

XML

PubMed Links

Search on Google