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Incontinentia pigmenti (Bloch–Sulzberger syndrome)

2015
Incontinentia pigmenti (IP; Bloch-Sulzberger syndrome; OMIM #308300) is an X-linked dominant neurocutaneous disorder with presumed male lethality. It is usually diagnosed in female newborns based on skin features (erythematous, vesicular, or bullous eruption in linear streaks).
Mohan J, Narayanan   +2 more
openaire   +2 more sources

735 Syndrome de Bloch-Sulzberger

Journal Français d'Ophtalmologie, 2007
Introduction Le syndrome de Bloch-Sulzberger, ou incontinentia pigmenti, est une genodermatose pigmentaire, de transmission dominante liee a l’X, qui affecte surtout les filles. Elle est souvent letale chez les garcons. C’est une maladie rare. Les manifestations oculaires existent dans 25 a 35 % des cas.
S. Goulmam   +8 more
openaire   +1 more source

[Bloch-Sulzberg syndrome in pathology].

Ceskoslovenska patologie, 2007
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 ...
K, Adamicová   +3 more
openaire   +1 more source

Bloch-Sulzberger Syndrome

2009
Alexander K. C. Leung   +62 more
openaire   +1 more source

A Case of Bloch-Sulzberger Syndrome

Nishi Nihon Hifuka, 2016
Satoko NAKASHIMA   +5 more
openaire   +1 more source

Bloch-Sulzberger syndrome - case report

2015
Bloch-Sulzberger (BS) sindrom ili Incontinentia pigmenti rijedak je genetski poremećaj razvoja ektodermalnih struktura. Nasljeđuje se X-vezano dominantno i uglavnom pogađa ženski spol s različitom ekspresijom, dok je za muški spol većinom letalan intrauterino. U većine oboljelih javlja se de-novo.
Paučić-Kirinčić, Ela   +5 more
openaire  

A Case Report of a Bloch-sulzberger Syndrome (Incontinentia Pigmenti) Patient on Whom We Performed Orthognathic Surgery under General Anesthesia

Japanese Journal of Oral Diagnosis / Oral Medicine, 2016
Akinori Moroi   +2 more
exaly  

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