Immune system disturbances in Clouston syndrome

Author:

Pietrzak Aldona1,Grywalska Ewelina2,Gerkowicz Agnieszka1,Krasowska Dorota1,Chodorowska Grażyna1,Michalska‐Jakubus Małgorzata1,Roliński Jacek2,Wawrzycki Bartłomiej1,Radej Sebastian3,Dybiec Ewa4,Wroński Jacek5,Sobczyńska‐Tomaszewska Agnieszka6,Rudzki Marcin7,Hadj‐Rabia Smail8

Affiliation:

1. Department of Dermatology, Venereology and Pediatric Dermatology Medical University of Lublin Lublin Poland

2. Department of Clinical Immunology and Immunotherapy Medical University of Lublin Lublin Poland

3. Department of Human Anatomy Medical University of Lublin Lublin Poland

4. Department of Pediatric Radiology Medical University of Lublin Lublin Poland

5. Department of Vascular Surgery and Angiology Medical University of Lublin Lublin Poland

6. Health Care Centre MedGen Warsaw Poland

7. Department of Maxillofacial Orthopedics Medical University of Lublin Lublin Poland

8. Department of Dermatology Hôpital Universitaire Necker‐Enfants Malades Paris France

Funder

Medical University of Lublin Research

Publisher

Wiley

Subject

Dermatology

Reference28 articles.

1. Hydrotic ectodermal dysplasia – Clouston's family revisited;Williams M;Can Med Assoc J,1967

2. Clouston Syndrome Can Mimic Pachyonychia Congenita

3. A novelGJB6missense mutation in hidrotic ectodermal dysplasia 2 (Clouston syndrome) broadens its genotypic basis

4. Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping

5. ZambrunoG.Clouston syndrome[WWW document] 2008.http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=189(accessed 22 February 2014).

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