Biemond syndrome | |
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Other names | Brachydactyly–nystagmus–cerebellar ataxia syndrome |
Biemond syndrome is a genetic disorder characterised by brachydactyly, nystagmus, strabismus, cerebellar ataxia and intellectual disability.
The 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]
![]() | This section is empty. You can help by
adding to it. (January 2018) |
![]() | This section is empty. You can help by
adding to it. (January 2018) |
It was first described in 1934 by Dutch neurologist Arie Biemond (1902–1973). It has not been described since. [1] [2]
Biemond syndrome | |
---|---|
Other names | Brachydactyly–nystagmus–cerebellar ataxia syndrome |
Biemond syndrome is a genetic disorder characterised by brachydactyly, nystagmus, strabismus, cerebellar ataxia and intellectual disability.
The 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]
![]() | This section is empty. You can help by
adding to it. (January 2018) |
![]() | This section is empty. You can help by
adding to it. (January 2018) |
It was first described in 1934 by Dutch neurologist Arie Biemond (1902–1973). It has not been described since. [1] [2]