Bloch-Sulzberg Syndrome in Pathology
Authors:
K. Adamicová 1; Ž. Fetisovová 2; V. Máliš 3; S. Málišová 2
Authors‘ workplace:
Ústav patologickej anatómie, 2Kožná klinika a 3Očná klinika
Jesseniova lekárska fakulta v Martine Univerzity Komenského v Bratislave a Martinská
fakultná nemocnica v Martine
1
Published in:
Čes.-slov. Patol., 43, 2007, No. 3, p. 109-113
Category:
Original Article
Overview
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).
Key words:
Bloch-Sultzberg syndrom – incontitentia pigmenti – histology of the skin – pilli bifurcati
Labels
Anatomical pathology Forensic medical examiner ToxicologyArticle was published in
Czecho-Slovak Pathology
2007 Issue 3
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