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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Detalles Bibliográficos
Autores principales: Weiss, Stephanie J., Srinivasan, Archana, Klufas, Michael A., Shields, Carol L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5603187/
https://www.ncbi.nlm.nih.gov/pubmed/28932485
http://dx.doi.org/10.1186/s40942-017-0088-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5603187/
https://www.ncbi.nlm.nih.gov/pubmed/28932485
http://dx.doi.org/10.1186/s40942-017-0088-5

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