ORPHA:2078
Geroderma osteodysplastica
- Body system
- Skin diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:2078 is classified under "Skin diseases" in the Orphanet nomenclature.
Common signs
- Joint hypermobility
- Osteoporosis
- Thin skin
- Hyperextensible skin
- Redundant skin
- Recurrent fractures