Netherton syndrome associated with idiopathic congenital hemihypertrophy

Pediatric Dermatology

Volumn 19, Issue 4, 2002, Pages 345-348

  Yerebakan, Özlem ^a   Uǧuz, Ayşen ^a   Keser, Ibrahim ^a   Lüleci, Güven ^a   Çiftçioǧlu, Mehmet Akif ^a   Başaran, Erdal ^a   Alpsoy, Erkan ^a  

^a AKDENIZ UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; ATOPY; CASE REPORT; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CLINICAL FEATURE; DERMATITIS; DISEASE ASSOCIATION; FEMALE; FOLLOW UP; GROWTH RETARDATION; HEMIHYPERTROPHY; HISTOPATHOLOGY; HUMAN; IDIOPATHIC DISEASE; KIDNEY SIZE; LABORATORY TEST; NETHERTON DISEASE; PHYSICAL EXAMINATION; PRESCHOOL CHILD; PRIORITY JOURNAL; SKIN BIOPSY;

ABNORMALITIES, MULTIPLE; BIOPSY, NEEDLE; BONE AND BONES; DERMATITIS, ATOPIC; DEVELOPMENTAL DISABILITIES; FEMALE; HAIR; HUMANS; ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL; IMMUNOHISTOCHEMISTRY; INFANT; PROGNOSIS; RISK ASSESSMENT; SCALP DERMATOSES; SKIN ABNORMALITIES; SYNDROME;

EID: 0036657047     PISSN: 07368046     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1525-1470.2002.00098.x     Document Type: Article

References (21)

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3. Syndrome de Netherton. Aspects actuels. A propos de neuf cas
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5. Helical hairs: A new hair anomaly in a patient with Netherton's syndrome
6. Neonatal hypernatremia in two siblings with Netherton's syndrome
7. Manifestations digestives et nutritionnelles du syndrome de Netherton
8. Netherton's syndrome in a male
9. Ichthyosis linearis circumflexa Comél with trichorrhexis invaginata (Netherton's syndrome): A light microscopical study of the skin changes
10. Normal liver, spleen, and kidney dimensions in neonates, infants, and children: Evaluation with sonography
11. Manifestations and natural history of idiopathic hemihypertrophy: A review of eleven cases
12. Idiopathic congenital hemihypertrophy with associated ipsilateral benign nephromegaly
13. Hemihypertrophy, concepts and controversies
14. Isolated hemihyperplasia (hemihypertrophy): Report of a prospective multicenter study of the incidence of neoplasia and review
15. Congenital hemihypertrophy. Tendency to association with other abnormalities and/or tumors
16. Congenital hemihypertrophy associated with cutaneous pigmento-vascular, cerebral, visceral and bone abnormalities
17. Linear nevi, hemihypertrophy, connective tissue hamartomas, and unusual neoplasms in children
18. Wilms's tumor in three children of a woman with congenital hemihypertrophy
19. Wilm's tumour and congenital hemihypertrophy: Report of 5 new cases and review of literature
20. Localization of the Netherton syndrome gene to chromosome 5q32, by linkage analysis and homozygosity mapping
21. Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome