Multiple synostoses syndrome 1
From WikiMD's WELLNESSPEDIA
Other Names: Synostoses multiple with brachydactyly; Symphalangism brachydactyly syndrome; WL syndrome; Deafness-symphalangism syndrome of Herrmann; Facioaudiosymphalangism syndrome; SYNS1
Multiple synostoses syndrome (MSS) is a rare developmental bone disorder characterized by proximal symphalangism of the fingers and/or toes often associated with fusion of carpal and tarsal, humeroradial, and cervical spine joints.
NIH genetic and rare disease info[edit]
Multiple synostoses syndrome 1 is a rare disease.
| Rare and genetic diseases | ||||||
|---|---|---|---|---|---|---|
|
Rare diseases - Multiple synostoses syndrome 1
|