Incontinentia pigmenti in a child with suspected retinoblastoma

Incontinentia pigmenti in a child with suspected retinoblastoma

Abstract 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 trac...

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Bibliographic Details
Main Authors: Stephanie J. Weiss, Archana Srinivasan, Michael A. Klufas, Carol L. Shields
Format: Article
Language:English
Published: BMC 2017-09-01
Series:International Journal of Retina and Vitreous
Subjects:
Eye
Incontinentia pigmenti
Bloch–Sulzberger syndrome
Retinoblastoma
Pseudoretinoblastoma
Retinal detachment
Online Access:http://link.springer.com/article/10.1186/s40942-017-0088-5

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http://link.springer.com/article/10.1186/s40942-017-0088-5

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