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Alopecia antibody deficiency
A rare primary immunodeficiency disorder characterized by the association of alopecia areata totalis and antibody deficiency (congenital agammaglobulinemia or incomplete antibody deficiency syndrome), manifesting with recurrent infections. There have been no further descriptions in the literature since 1976.
ORPHA:1006
Classification level: Disorder
- Ipp-Gelfand syndrome
Source: PubMed ID 978318
Prevalence: <1 / 1 000 000
Inheritance: Unknown
Age of onset: Childhood, Infancy
ICD-10: D80.8
UMLS: C5190867
: produced/endorsed by ERN(s)
: produced/endorsed by FSMR(s)
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- Research project(s) (46)
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Newborn screening