Netherton Syndrome Associated with Growth Hormone Deficiency

Author:

Aydın Banu Küçükemre1,Baş Firdevs1,Tamay Zeynep2,Kılıç Gürkan2,Süleyman Ayşe2,Bundak Rüveyde1,Saka Nurçin1,Özkaya Esen3,Güler Nermin2,Darendeliler Feyza1

Affiliation:

1. Department of Pediatrics, Pediatric Endocrinology Unit; Istanbul Faculty of Medicine; Istanbul University; Istanbul Turkey

2. Department of Pediatrics; Pediatric Allergy Unit; Istanbul Faculty of Medicine; Istanbul University; Istanbul Turkey

3. Department of Dermatology; Istanbul Faculty of Medicine; Istanbul University; Istanbul Turkey

Publisher

Wiley

Subject

Dermatology,Pediatrics, Perinatology, and Child Health

Reference14 articles.

1. Netherton's syndrome: a syndrome of elevated IgE and characteristic skin and hair findings;Smith;J Allergy Clin Immunol,1995

2. Localization of the Netherton syndrome gene to chromosome 5q32, by linkage analysis and homozygosity mapping;Chavanas;Am J Human Genet,2000

3. Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome;Chavanas;Nat Genet,2000

4. Netherton syndrome: report of identical twins presenting severe atopic dermatitis;Kilic;Eur J Pediatr,2006

5. Diagnosis of growth hormone deficiency: the role of growth hormone (GH), insulin like growth factor (IGF-I) and IGF-binding protein (IGFBP-3);Bereket;J Clin Res Ped Endo,2009

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