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Incontinentia pigmenti [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2014
Incontinentia pigmenti is a rare genodermatosis in which the skin involvement occurs in all patients. Additionally, other ectodermal tissues may be affected, such as the central nervous system, eyes, hair, nails and teeth.
Claudia Schermann Poziomczyk   +12 more
doaj   +8 more sources

Incontinentia pigmenti

open access: yesIndian Journal of Pathology and Microbiology, 2010
Incontinentia pigmenti (IP) or Bloch-Sulzberger syndrome is a rare X-linked dominant genodermatosis related to the NF kappa B essential modulator (NEMO) gene with approximately 800 cases reported worldwide.
Motamedi Mohammad Hosein   +4 more
doaj   +7 more sources

Incontinentia pigmenti

open access: yesJournal of Indian Society of Pedodontics and Preventive Dentistry, 2006
Incontinentia pigmenti or Bloch-Sulzberger syndrome, is a rare X linked dominant disorder with characteristic skin, hair, eye, dental and neurological abnormalities commonly affecting females.
Hegde Sundeep, Bhat S, Soumya S, Pai D
doaj   +4 more sources

Case Report: Diagnosis and treatment of incontinentia pigmenti with central nervous system anomalies in one patient [PDF]

open access: yesFrontiers in Pediatrics
IntroductionThis article reports a detailed case of a patient with incontinentia pigmenti who exhibited epileptic status and dermatologic symptoms.Case presentationA 5-month-old female patient was brought to our hospital due to status epilepticus, with ...
Yun Li   +6 more
doaj   +2 more sources

Severe COVID-19 and long COVID in a 31-year-old woman with incontinentia pigmenti: A case report

open access: yesSAGE Open Medical Case Reports, 2021
Incontinentia pigmenti is a rare genetic disease affecting the skin, microvasculature, and central nervous system, in which a hyperactive inflammatory response is observed.
Sylvie Rheault
doaj   +1 more source

Incontinentia Pigmenti: A Rare Genodermatosis in a Male Child [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2015
Incontinentia pigmenti is rare X-linked dominant disorder. There is no consistent expression of Incontinetia pigmenti in female child, but in male child, they always lead to death in utero.
Dinesh Kumar Narayana Swamy   +3 more
doaj   +1 more source

Rimski steber z rdeče barvanim ometom iz Emone

open access: yesArheološki Vestnik, 2020
Arheološka izkopavanja, ki so leta 1999 potekala v Ljubljani, v inzuli XXVII Emone, so odkrila ostanek trupa stebra z organskim jedrom, postavljenega na kamnito plinto.
Andreja Maver   +4 more
doaj   +1 more source

Magnetic resonance imaging for diagnosing a rare disease: incontinentia pigmenti (Bloch–Sulzberger syndrome) on the example of a clinical case [PDF]

open access: yesDigital Diagnostics, 2023
Incontinentia pigmenti, also known as Bloch–Sulzberger syndrome, is a rare hereditary disease characterized by typical skin rashes and involvement of other organs and systems.
Igor I. Yarmola   +8 more
doaj   +1 more source

Incontinencia pigmenti. Estudio descriptivo de la experiencia en dos centros hospitalarios

open access: yesAnales de Pediatría, 2020
Resumen: Introducción: La incontinencia pigmenti es una genodermatosis poco frecuente, de herencia ligada al cromosoma X, que afecta a tejidos derivados del ectodermo. Nuestro objetivo es revisar de la forma más completa posible los casos diagnosticados
Sergio Ocaña Jaramillo   +2 more
doaj   +1 more source

Incontinentia pigmenti. A descriptive study of experience in two different hospitals

open access: yesAnales de Pediatría (English Edition), 2020
Introduction: Incontinentia pigmenti is a rare genodermatosis of inheritance linked to the X chromosome that affects tissues derived from ectoderm. The aim of the study is to review, as completely as possible, the cases diagnosed in paediatric patients ...
Sergio Ocaña Jaramillo   +2 more
doaj   +1 more source

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