An unusual presentation of immunodeficiency with hyper-IgM.
Pediatr Dermatol
; 18(1): 48-50, 2001.
Article
en En
| MEDLINE
| ID: mdl-11207972
Hyper-IgM syndrome is a rare immunodeficiency disease characterized by markedly decreased serum IgG, IgA, and IgE levels but normal or elevated IgM levels. The most common clinical signs are infections, cirrhosis, arthritis, malignancies, and mucosal ulcers. Approximately two-thirds of patients have chronic neutropenia associated with oral and perirectal ulcers. We report a 14-month-old girl with hyper-IgM syndrome who has recurrent cutaneous ulcers restricted to the diaper area.
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Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Úlcera Cutánea
/
Inmunoglobulina M
/
Disgammaglobulinemia
Tipo de estudio:
Diagnostic_studies
Límite:
Female
/
Humans
/
Infant
Idioma:
En
Revista:
Pediatr Dermatol
Año:
2001
Tipo del documento:
Article
País de afiliación:
Turquía