Results 11 to 20 of about 201 (96)
Incontinencia pigmenti en un recién nacido. Presentación de un caso
Medisur, 2015 La incontinentia pigmenti, también conocida como síndrome de Bloch-Sulzberger, es un síndrome neurocutáneo de herencia dominante ligada al cromosoma X, con una variable afectación de tejidos derivados del neuroectodermo y mesodermo: piel, faneras, ojos ...
Yahiris García Rodríguez +1 more
doaj +1 more source
Incontinencia pigmenti: ¿es una entidad más grave en los varones? Reporte de 2 casos
Actas Dermo-Sifiliográficas, 2022 V. Vezzaro +3 more
doaj +2 more sources
Incontinencia pigmentaria [PDF]
, 2022 Incontinentia Pigmenti is a rare genodermatosis, which is considered a hereditary alteration, linked to the X chromosome, with a dominant character. It occurs more frequently in women, and the main involvement is observed in tissues derived from the ...
Contreras Gala, Katherine Luisa +2 more
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Incontinencia Pigmenti: una genodermatosis de comienzo en la infancia [PDF]
, 2021 Introduction: incontinentia pigmenti is a dominant inheritance genodermatosis, with an approximate incidence of 1 per 50 000 live births, with 27.6 new cases per year.Objective: to describe the main clinical and histopathological characteristics of ...
Espin Guerra, Leydiani +2 more
core +3 more sources
Incontinentia pigmenti. A descriptive study of experience in two different hospitals
Anales 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
Incontinencia pigmenti en madre e hija: Relato de caso clínico [PDF]
Revista chilena de pediatría, 2011 ABSTRACTMother and daughter incontinentia pigmenti. Case report Incontinentia pigmenti (IP) is a rare genodermatosis linked to the X chromosome. It affects variably all tissues derives from neuroecthoderm such as skin, hair, nails, eyes and central nervous system. Early diagnosis allows the study of eventual multisystem involvement.
Mª LEONOR ENEI G +4 more
openaire +2 more sources
Manifestaciones orales de la incontinencia pigmentaria (Síndrome de BlochSulzberger). Reporte de caso [PDF]
, 2019 Paciente de sexo femenino de 13 años de edad que acudió al servicio de Odontopediatría del Instituto de Salud Oral del Hospital Central de la Fuerza Aérea de Perú en el mes de setiembre del año 2018 debido a una renovación en la prótesis parcial ...
Castro Rodríguez, Yuri +2 more
core +4 more sources
Actas Dermo-Sifiliográficas, 2019 Incontinentia pigmenti (Bloch-Sulzberger syndrome) is a rare neuroectodermal dysplasia. It is an X-linked dominant disorder caused by mutations in the IKBKG/NEMO gene on Xq28. Approximately 80% of patients have a deletion of exons 4 to 10. Incontinentia pigmenti has an estimated incidence of 0.7 cases per 100,000 births.
CammarataScalisi F, Fusco F, Ursini M V
openaire +5 more sources
, 2011 O termo úlcera de Marjolin é usado para designar a transformação maligna que se origina na pele cronicamente lesada. Trata-se de neoplasia mais agressiva do que aquelas não relacionadas com cicatriz e, frequentemente, é subdiagnosticada ou tratada de ...
ALMEIDA, José Roberto Paes de +4 more
core +3 more sources
Anais Brasileiros de Dermatologia, 2010 A incontinência pigmentar é uma genodermatose rara, ligada ao X, que afeta, principalmente, neonatos do sexo feminino. As manifestações cutâneas são as mais prevalentes, e ocorrem em quatro fases bem distintas. Lactente feminina com lesões vesicobolhosas
Marcela A. C. Pereira +4 more
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