Incontinentia pigmenti (Bloch-Sulzberger syndrome): seven case reports from one family.
AUTOR(ES)
Spallone, A
RESUMO
Seven members from a large family who showed signs of incontinentia pigmenti were examined. A clear X-linked dominant transmission was demonstrated, lethal in males. Study of this family shows that vascular abnormalities of the retina and disorders of the retinal pigment epithelium are the most important ocular lesions in the Bloch-Sulzberger syndrome.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1041246Documentos Relacionados
- Fundus changes in incontinentia pigmenti (Bloch-Sulzberger syndrome): a case report.
- Incontinentia pigmenti (Bloch-Sulzberger syndrome).
- Incontinentia pigmenti (Bloch-Sulzberger syndrome) and retinal changes.
- Bloch-Sulzberger Syndrome (incontinentia pigmenti).
- Incontinentia pigmenti or Bloch-Sulzberger syndrome: a rare X-linked genodermatosis