Mirhosseini–Holmes–Walton syndrome
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| Mirhosseini–Holmes–Walton syndrome | |
|---|---|
| Other names | Pigmentary retinopathy-intellectual disability syndrome |
| Specialty | Ophthalmology, Neurology |
Mirhosseini–Holmes–Walton syndrome is a syndrome which involves retinal degeneration, cataract, microcephaly, and mental retardation. It was first characterized in 1972. There is evidence that this syndrome has a different mutation in the same gene as Cohen syndrome.