OMIM 268050 | DiseasesDB 32623 | |
Mirhosseini–Holmes–Walton syndrome is a syndrome which involves retinal degeneration, cataract, microcephaly, and mental retardation. It was first characterized in 1972.
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.
References
Mirhosseini–Holmes–Walton syndrome Wikipedia(Text) CC BY-SA