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The Ohdo blepharophimosis syndrome: a third case.
A patient with a syndrome consisting of blepharophimosis, simple ears, hypoplastic teeth, developmental delay, and hypotonia is described. Previous case reports are reviewed and a differential diagnosis is described. Many of the features in the subject are similar to those described in two previous...
Sparad:
| I publikationen: | J Med Genet |
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| Huvudupphovsman: | |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
BMJ Publishing Group
1991
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1016784/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2002485/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.28.2.131 |
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