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Incontinentia pigmenti (Bloch–Sulzberger syndrome)
2015Incontinentia 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
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735 Syndrome de Bloch-Sulzberger
Journal Français d'Ophtalmologie, 2007Introduction 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
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[Bloch-Sulzberg syndrome in pathology].
Ceskoslovenska patologie, 2007The 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
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Retinoblastoma in Bloch-Sulzberger Syndrome
Ophthalmologica, 2010J, Blake, J, Mullaney
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A Case of Bloch-Sulzberger Syndrome
Nishi Nihon Hifuka, 2016Satoko NAKASHIMA +5 more
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Bloch-Sulzberger syndrome - case report
2015Bloch-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
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The Bloch-Sulzberger syndrome in an English family.
British Journal of Dermatology, 1963openaire +2 more sources

