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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
exaly   +4 more sources

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
exaly   +3 more sources

NEMO Gene Mutations in Chinese Patients With Incontinentia Pigmenti

open access: yesJournal of the Formosan Medical Association, 2010
Incontinentia pigmenti is a rare, X-linked, dominant genodermatosis affecting skin, teeth, eyes, and central nervous system. Symptoms are associated with mutations in the nuclear factor-kappa B essential modulator (NEMO) gene on chromosome Xq28.

exaly   +3 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

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

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

Biodeterioration and chemical conservation of Bhimkichak Temple, Malhar, Chhattisgarh, India

open access: yesConservation Science in Cultural Heritage, 2012
Stone cultural heritage materials are at risk of bio-deterioration caused by diverse populations of microorganisms living in biofilms. The microbial metabolites of these biofilms are responsible for the deterioration of the underlying substratum and may ...
Sanjay Prasad Gupta   +2 more
doaj   +1 more source

Kapoyt/blu: alla scoperta della storia armena di un colore

open access: yesLanx, 2012
The study begins with an analysis of the semantics of the Armenian word kapoyt, blue, taking into account its different uses in Armenian literature, e.g.
Marco Bais
doaj   +1 more source

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