ORPHA:1006
Alopecia antibody deficiency
Also called Ipp-Gelfand syndrome
- Body system
- Skin diseases
- Inheritance pattern
- Unknown
- Typical age of onset
- Childhood, Infancy
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:1006 is classified under "Skin diseases" in the Orphanet nomenclature.
Common signs
- Abnormal eyelash morphology
- Recurrent respiratory infections
- Sparse body hair
- Immunodeficiency
- Decreased circulating antibody level
- Sparse hair