Severe visual impairment and retinal changes in a boy with a deletion of the gene for Nance-Horan syndrome.
2007
We present the ophthalmologic findings in a boy with a deletion of Xp22 comprising the gene for NanceHoran syndrome. Different mechanisms underlying the visual impairment in Nance-Horan syndrome are discussed.
Keywords:
- Correction
- Source
- Cite
- Save
- Machine Reading By IdeaReader
6
References
4
Citations
NaN
KQI