1.
Cesk Patol
; 43(3): 109-13, 2007 Jul.
Article
in Slovak
| MEDLINE
| ID: mdl-17821839
ABSTRACT
The authors present some pathological findings in the skin and hair of the child affected by rather rare Bloch-Sulzberg syndrome manifested in incontinentia pigmenti, followed for 10 years. In this work are presented also some recent data about pathogenesis of the disease with X-chromosome dominant heredity, primary of neuroectodermal origincaused by mutation of nuclear factor kappa-B of essential modulator (NEMO) of the gene (chromosomal locus Xq28).
Subject(s)
Incontinentia Pigmenti/pathology , Child , Female , Humans , Skin/pathology
2.
Acta Derm Venereol
; 75(3): 244, 1995 May.
Article
in English
| MEDLINE
| ID: mdl-7653189