Gerodermia osteodysplastica
| Gerodermia osteodysplastica | |
|---|---|
| Other names | Geroderma osteodysplasticum and Walt Disney dwarfism | 
| Gerodermia osteodysplastica has an autosomal recessive pattern of inheritance. | |
| Specialty | Medical genetics | 
Gerodermia osteodysplastica (GO) is a rare autosomal recessive connective tissue disorder included in the spectrum of cutis laxa syndromes.
This condition is inherited in an autosomal recessive pattern and leads to a range of skeletal abnormalities and skin changes.
Usage of the name "Walt Disney dwarfism" is attributed to the first known case of the disorder, documented in a 1950 journal report, in which the authors described five affected members from a Swiss family as having the physical appearance of dwarves from a Walt Disney film.
The terms "geroderma" or "gerodermia" can be used interchangeably with "osteodysplastica" or "osteodysplasticum", with the term "hereditaria" sometimes appearing at the end.