Olmsted syndrome: Exploration of the immunological phenotype

Orphanet Journal of Rare Diseases

Volumn 8, Issue 1, 2013, Pages

  Danso Abeam, Dina ^a,b   Zhang, Jianguo ^c,d   Dooley, James ^a,b   Staats, Kim A ^a,b   Van Eyck, Lien ^a,b   Van Brussel, Thomas ^e   Zaman, Shari ^a,b   Hauben, Esther ^f   Van De Velde, Marc ^f   Morren, Marie Anne ^f   Renard, Marleen ^f   Van Geet, Christel ^f   Schaballie, Heidi ^f   Lambrechts, Diether ^e   Tao, Jinsheng ^d   Franckaert, Dean ^a,b   Humblet Baron, Stephanie ^a,b   Meyts, Isabelle ^b,f   Liston, Adrian ^a,b  

^a DEPARTMENT OF PLANT SYSTEMS BIOLOGY   (Belgium)

^b UNIVERSITY OF LEUVEN   (Belgium)

^c FUDAN UNIVERSITY   (China)

^d BGI SHENZHEN   (China)

^e University of Leuven   (Belgium)

^f UNIVERSITY HOSPITALS LEUVEN   (Belgium)

Author keywords

Eosinophil; Follicular T cell; IgE; Olmsted syndrome; TRPV3

Indexed keywords

IMMUNOGLOBULIN E; VANILLOID RECEPTOR 3;

ADULT; ARTICLE; CASE REPORT; EOSINOPHIL COUNT; EOSINOPHILIA; HUMAN; HYPER IGE SYNDROME; IMMUNE DYSREGULATION; IMMUNOGLOBULIN PRODUCTION; IMMUNOPHENOTYPING; INFLAMMATORY INFILTRATE; LYMPHOCYTE COUNT; MALE; OLMSTED SYNDROME; POINT MUTATION; SKIN INFECTION;

ADULT; EOSINOPHILIA; FACIAL DERMATOSES; FEMALE; HUMANS; HYPERPLASIA; IMMUNOGLOBULIN E; KERATODERMA, PALMOPLANTAR; KERATOSIS; MALE; MUTATION; PHENOTYPE; SKIN; SYNDROME; TRPV CATION CHANNELS; YOUNG ADULT;

EID: 84877887353     PISSN: None     EISSN: 17501172     Source Type: Journal    
DOI: 10.1186/1750-1172-8-79     Document Type: Article

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