Nezelof syndrome
Nezelof syndrome | |
ICD-10 | D81.4 |
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ICD-9 | 279.13 |
OMIM | 242700 |
DiseasesDB | 29571 |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
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Overview
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 was considered a form of combined immunodeficiency in ICD-10 but a deficiency of cell-mediated immunity in ICD-9.
References
- ↑ Online Mendelian Inheritance in Man (OMIM) 242700
- ↑ Nezelof C, Jammet ML, Lortholary P, Labrune B, Lamy M (1964). "Hereditary Thymic Hypoplasia: Its Place And Responsibility In A Case Of Lymphocytic, Normoplasmocytic And Normoglobulinemic Aplasia In An Infant" (Free full text). Archives francaises de pediatrie. 21: 897–920. ISSN 0003-9764. PMID 14195287. Unknown parameter
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