Ophthalmological findings in series of incontinentia pigmenti patients from Serbia

Ophthalmological findings in series of incontinentia pigmenti patients from Serbia

Introduction. Incontinentia pigmenti (IP) is a rare complex X-linked genodermatosis in which skin changes are combined with anomalies of other organs. Mutations of the NEMO gene localized on chromosome Xq28 are responsible for IP. Clinical manifestations of IP according to evolution and prognosis ca...

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Bibliographic Details
Main Authors: Minić Snežana, Novotny Gerd E.K., Stefanović Ivan, Obradović Miljana, Trpinac Dušan
Format: Article
Language:English
Published: Serbian Medical Society 2010-01-01
Series:Srpski Arhiv za Celokupno Lekarstvo
Subjects:
incontinentia pigmenti
ocular anomalies
microphthalmia
cataract
nystagmus
strabismus
Online Access:http://www.doiserbia.nb.rs/img/doi/0370-8179/2010/0370-81791004150M.pdf

Internet

http://www.doiserbia.nb.rs/img/doi/0370-8179/2010/0370-81791004150M.pdf

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