Under‐recognition of acral peeling skin syndrome: 59 new cases with 15 novel mutations-Reference-Cited by-同舟云学术

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

Published:2014-10-20 Issue:5 Volume:171 Page:1206-1210
ISSN:0007-0963
Container-title:British Journal of Dermatology
language:en
Short-container-title:Br J Dermatol

Author:

Szczecinska W.¹,Nesteruk D.²,Wertheim‐Tysarowska K.²,Greenblatt D.T.³,Baty D.⁴,Browne F.¹,Liu L.⁵,Ozoemena L.⁵,Terron‐Kwiatkowski A.⁴,McGrath J.A.⁶,Mellerio J.E.³⁷,Morton J.⁸,Woźniak K.⁹,Kowalewski C.⁹,Has C.¹⁰,Moss C.¹

Affiliation:

1. Department of Dermatology Birmingham Children's Hospital Steelhouse Lane Birmingham B4 6NH U.K

2. Department of Medical Genetics Institute of Mother and Child Warsaw Poland

3. St John's Institute of Dermatology Guy's and St Thomas' NHS Foundation Trust London U.K

4. East of Scotland Regional Genetics Service Ninewells Hospital Dundee U.K

5. GSTS Pathology St Thomas' Hospital London U.K

6. St John's Institute of Dermatology King's College London (Guy's Campus) London U.K

7. Great Ormond Street Hospital for Children NHS Foundation Trust London U.K

8. West Midlands Clinical Genetics Service Birmingham Women's Hospital Birmingham U.K

9. Department of Dermatology and Immunodermatology Medical University of Warsaw Warsaw Poland

10. Department of Dermatology University Medical Center Freiburg Freiburg Germany

Funder

German Research Council

Publisher

Wiley

Subject

Dermatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjd.12964

Reference15 articles.

1. Acral Peeling Skin Syndrome: A Clinically and Genetically Heterogeneous Disorder

2. Acral Peeling Skin Syndrome Resulting from a Homozygous Nonsense Mutation in theCSTAGene Encoding Cystatin A

3. TGM5 Mutations Impact Epidermal Differentiation in Acral Peeling Skin Syndrome

4. A recurrent mutation in the TGM5 gene in European patients with acral peeling skin syndrome

5. Acral Peeling Skin Syndrome Resembling Epidermolysis Bullosa Simplex in a 10-Month-Old Boy

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