ORPHA:1159
Progressive pseudorheumatoid dysplasia
Also called PPD, Progressive pseudorheumatoid arthropathy of childhood, Spondyloepiphyseal dysplasia tarda-progressive arthropathy syndrome
- Body system
- Bone diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Childhood
- Estimated prevalence
- 1-9 / 1 000 000 (Europe)
- Rarity class
- 1-9 / 1 000 000
ORPHA:1159 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- Platyspondyly
- Joint swelling
- Waddling gait
- Spondyloepiphyseal dysplasia
- Irregular vertebral endplates
- Narrow small joints of the hand