Nezelof syndrome
From Wikipedia, the free encyclopedia
| Nezelof syndrome Classification and external resources |
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| ICD-10 | D81.4 |
|---|---|
| ICD-9 | 279.13 |
| OMIM | 242700 |
| DiseasesDB | 29571 |
Nezelof syndrome (a form of thymic dysplasia) is an autosomal recessive[1] congenital immunodeficiency condition due to underdevelopment of the thymus.
It was characterized in 1964.[2]
It considered a form of combined immunodeficiency in ICD-10 but a deficiency of cell-mediated immunity in ICD-9.
[edit] External links
[edit] References
- ^ Online 'Mendelian Inheritance in Man' (OMIM) 242700
- ^ NEZELOF C, JAMMET ML, LORTHOLARY P, LABRUNE B, LAMY M (October 1964). "[HEREDITARY THYMIC HYPOPLASIA: ITS PLACE AND RESPONSIBILITY IN A CASE OF LYMPHOCYTIC, NORMOPLASMOCYTIC AND NORMOGLOBULINEMIC APLASIA IN AN INFANT.]" (in French). Arch. Fr. Pediatr. 21: 897–920. PMID 14195287.
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