Incontinentia pigmenti with secondary Raynaud's phenomenon: A case report and review of the literature-Reference-Cited by-同舟云学术

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Incontinentia pigmenti with secondary Raynaud's phenomenon: A case report and review of the literature

Published:2017-06 Issue: Volume:6 Page:27-29
ISSN:2451-9936
Container-title:American Journal of Ophthalmology Case Reports
language:en
Short-container-title:American Journal of Ophthalmology Case Reports

Author:

Greven Margaret A.,Moshfeghi Darius M.

Publisher

Elsevier BV

Subject

Ophthalmology

Reference12 articles.

1. Incontinentia pigmenti: a comprehensive review and update;Swinney;OSLI Retina,2015

2. Insights into IKBKG/NEMO Locus: report of new mutations and complex genomic rearrangements leading to incontinentia pigmenti disease;Conte;Hum Mutat,2014

3. Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium;Smahi;Nature,2000

4. NEMO, NFkappaB signaling and incontinentia pigmenti;Nelson;Curr Opin Genet Dev,2006

5. Alterations of the IKBKG locus and diseases: an update and a report of 13 novel mutations;Fusco;Hum Mutat,2008

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