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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
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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 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
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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
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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
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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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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
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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
doaj +1 more source

