Multiple synostoses syndrome 1
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 source]
Multiple synostoses syndrome 1 is a rare disease.
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