Mirhosseini–Holmes–Walton syndrome
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| Mirhosseini–Holmes–Walton syndrome | |
|---|---|
| Classification and external resources | |
| Specialty | Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value). |
| OMIM | 268050 |
| DiseasesDB | 32623 |
| Patient UK | Mirhosseini–Holmes–Walton syndrome |
Mirhosseini–Holmes–Walton syndrome is a syndrome which involves retinal degeneration, cataract, microcephaly, and mental retardation. It was first characterized in 1972.[1][2]
The gene or genes involved have not yet been determined. There is some evidence that this syndrome has the same genetic cause as Cohen syndrome.[3]
References
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