Biemond syndrome is a genetic disorder characterised by brachydactyly, nystagmus, strabismus, cerebellar ataxia and intellectual disability.
| Biemond syndrome | |
|---|---|
| Other names | Brachydactyly–nystagmus–cerebellar ataxia syndrome |
Signs and symptoms
editThe family described by Biemond had a few members across four generations who had brachydactyly (due to one short metacarpal and metatarsal), nystagmus, strabismus, cerebellar ataxia and intellectual disability. Some of the members did not have the full syndrome.[1]
Diagnosis
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Treatment
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History
editIt was first described in 1934 by Dutch neurologist Arie Biemond (1902–1973). It has not been described since.[1][2]
References
edit- ^ a b "OMIM Entry - 113400 - BRACHYDACTYLY-NYSTAGMUS-CEREBELLAR ATAXIA". omim.org. Retrieved 2019-12-23.
- ^ Beighton, Greta (2012-12-06). The Person Behind the Syndrome. Springer Science & Business Media. p. 83. ISBN 978-1-4471-0925-9.
External links
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