Case Report: Diagnosis and treatment of incontinentia pigmenti with central nervous system anomalies in one patient [PDF]
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
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
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
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
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Incontinentia Pigmenti: A Rare Genodermatosis in a Male Child [PDF]
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
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Rimski steber z rdeče barvanim ometom iz Emone
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
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]
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
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Biodeterioration and chemical conservation of Bhimkichak Temple, Malhar, Chhattisgarh, India
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
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Kapoyt/blu: alla scoperta della storia armena di un colore
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
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