Incontinentia pigmenti: A propósito de un caso.

Authors

  • Tori Tori Carlos
  • Enriqueta Villar De Cipriani
  • Javier Arias Stella
  • Carmen Avalos

DOI:

https://doi.org/10.20453/rmh.v6i3.487

Abstract

Incontinentia Pigmenti is a rare X-linked multisystem neuroectodermic disorder with signs and symptoms related mainly to the dermatologic, dental, ocular and central nervous systems, and characterized by death in the majority of male embryos. Affected children do not appear sick, in spite of the skin eruption, the peripheral leucocytosis and marked eosinophilia. Most of the cases are reported in caucasians, although there are description in black children, orientals, north central and south american Indians, and in our mestizos. The name of Incontinentia Pigmenti describes the incontinence of the melanin pigment from the basal layer of the epidemermis into the superficial dermis.

Published

2013-08-20

How to Cite

1.
Carlos TT, Villar De Cipriani E, Arias Stella J, Avalos C. Incontinentia pigmenti: A propósito de un caso. Rev Méd Hered [Internet]. 2013 Aug. 20 [cited 2024 May 2];6(3). Available from: https://revistas.upch.edu.pe/index.php/RMH/article/view/487

Issue

Section

BRIEF COMUNICATION