ORPHA:300493
Sagliker syndrome
- Body system
- Bone diseases
- Inheritance pattern
- Multigenic/multifactorial
- Typical age of onset
- All ages
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:300493 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- Abnormality of the dentition
- Abnormal facial shape
- Elevated circulating parathyroid hormone level
- Short stature
- Depression
- Waddling gait