ORPHA:1014
Alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome
Also called Devriendt-Vandenberghe-Fryns syndrome
- Body system
- Skin diseases
- Inheritance pattern
- Unknown
- Typical age of onset
- Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:1014 is classified under "Skin diseases" in the Orphanet nomenclature.
Common signs
- Hypergonadotropic hypogonadism
- Intellectual disability, mild
- Alopecia totalis