ORPHA:1667
Wolcott-Rallison syndrome
Also called Early-onset diabetes mellitus with multiple epiphyseal dysplasia, WRS
- Body system
- Bone diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:1667 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- Neonatal insulin-dependent diabetes mellitus
- Abnormality of the liver
- Growth delay
- Skeletal dysplasia
- Short stature
- Decreased total neutrophil count