ORPHA:168621
Dysplasia of head of femur, Meyer type
Also called DECF, Dysplasia epiphysealis capitis femoris, Meyer dysplasia
- Body system
- Bone diseases
- Inheritance pattern
- Not documented in Orphadata
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- Unknown (Worldwide)
- Rarity class
- Unknown
ORPHA:168621 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- Delayed skeletal maturation
- Delayed femoral head ossification
- Multicentric femoral head ossification
- Increased total leukocyte count
- Waddling gait
- Elevated erythrocyte sedimentation rate