Incontinentia pigmenti (Bloch-Sulzberger syndrome) and retinal changes.
AUTOR(ES)
François, J
RESUMO
Incontinentia pigmenti is associated with various anomalies in 80% of cases. Among the most important are the ocular abnormalities and more particularly a retrolental mass with detachment of a dysplastic retina. At the basis of this manifestation are retinal vascular changes, characterised at first by ectatic tortuous veins and arteriovenous anastomoses as well as by aneurysmal-like dilatations.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1040231Documentos Relacionados
- Incontinentia pigmenti (Bloch-Sulzberger syndrome).
- Fundus changes in incontinentia pigmenti (Bloch-Sulzberger syndrome): a case report.
- Bloch-Sulzberger Syndrome (incontinentia pigmenti).
- Incontinentia pigmenti (Bloch-Sulzberger syndrome): seven case reports from one family.
- Incontinentia pigmenti or Bloch-Sulzberger syndrome: a rare X-linked genodermatosis
