ORPHA:3134
SCARF syndrome
- Body system
- Skin diseases
- Inheritance pattern
- X-linked recessive
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:3134 is classified under "Skin diseases" in the Orphanet nomenclature.
Common signs
- Joint hypermobility
- Posteriorly rotated ears
- Inguinal hernia
- Cryptorchidism
- Bifid scrotum
- Perineal hypospadias