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Incontinentia pigmenti in a child with suspected retinoblastoma
BACKGROUND: Incontinentia pigmenti is a rare X-linked dominant syndrome caused by mutation in the NEMO/IKKgamma gene, and characterized by a spectrum of cutaneous, ocular, neurologic and dental abnormalities. In the eye, findings include retinal vascular non-perfusion, occasionally with traction ret...
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| Publicado no: | Int J Retina Vitreous |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5603187/ https://ncbi.nlm.nih.gov/pubmed/28932485 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40942-017-0088-5 |
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