História natural das trissomias 13 e 18, após diagnóstico pré-natal em um hospital escola

História natural das trissomias 13 e 18, após diagnóstico pré-natal em um hospital escola

Show other versions (2)

Introdução: As trissomias 18 (T18) e Trissomia 13 (T13) são respectivamente a segunda e terceira causa mais comum de aneuploidias, com um aumento no diagnóstico dado o desenvolvimento de métodos e protocolos que incluem rastreio ecográfico e bioquímico, com a possibilidade de realizar um diagnóstico...

Full description

Bibliographic Details
Main Author:	Peña Duque, Julio Alejandro
Other Authors:	Magalhães, Jose Antonio de Azevedo
Format:	Others
Language:	Portuguese
Published:	2018
Subjects:	Trissomia Gravidez Diagnóstico pré-natal Amniocentese Natural outcome Amniocentesis Pré-natal diagnosis Edwards Syndrome Trisomy 18 Patau Syndrome Trisomy 13
Online Access:	http://hdl.handle.net/10183/172542

Similar Items

História natural das trissomias 13 e 18, após diagnóstico pré-natal em um hospital escola
by: Peña Duque, Julio Alejandro
Published: (2018)

História natural das trissomias 13 e 18, após diagnóstico pré-natal em um hospital escola
by: Peña Duque, Julio Alejandro
Published: (2018)

Patau Syndrome with Genotype 47,XY, + 13,t(13:18)
by: Vanda Elfira, et al.
Published: (2019-12-01)

West syndrome and mosaic trisomy 13: A case report
by: Hechmi Ben Hamouda, et al.
Published: (2018-05-01)

Adenocarcinoma and polyposis of the colon in a 20-year-old patient with Trisomy 13: a case report
by: Danielle P. Thurtle, et al.
Published: (2018-03-01)

Prenatal Diagnosis of Translocation 13;13 Patau Syndrome: Clinical Features of Two Cases
by: Pazarbaşi A, et al.
Published: (2008-01-01)

Óbito fetal em gestações únicas com diagnóstico de trissomias dos cromossomos 21,18 13 e monossomia do X
by: Vanessa Vigna Goulart
Published: (2014)

Óbito fetal em gestações únicas com diagnóstico de trissomias dos cromossomos 21,18 13 e monossomia do X
by: Goulart, Vanessa Vigna
Published: (2014)

Sclerocornea - A rare manifestation of full trisomy 13
by: Snehal Ganatra, et al.
Published: (2021-01-01)

Low-level mosaic trisomy 13 at amniocentesis associated with a favorable outcome in a pregnancy
by: Chih-Ping Chen, et al.
Published: (2020-11-01)

Prenatal diagnosis of low-level mosaicism for trisomy 13 at amniocentesis associated with a favorable outcome
by: Chih-Ping Chen, et al.
Published: (2017-12-01)

Estudo crítico da avaliação da maturidade fetal pela citologia do líquido âmnico: comparação com outros métodos A critical study of the evaluation of foetal maturity through citology of the amniotic fluid: comparison with other methods
by: Pedro Augusto Marcondes de Almeida, et al.
Published: (1975-09-01)

Síndrome de Patau: relato de um caso de trissomia completa do cromossomo 13
by: Ana Cecília Alves Amaral, et al.
Published: (2019-11-01)

Dandy–Walker syndrome with duplex kidney abnormalities in trisomy 18 – A rare case report
by: Tun-Jun Wang, et al.
Published: (2017-10-01)

Pancreatic hamartoma in a premature Trisomy 18 female
by: Patricia Isabel Delgado, et al.
Published: (2017-12-01)

Changing Clinical Presentations and Survival Pattern in Trisomy 18
by: Chien-Chou Hsiao, et al.
Published: (2009-08-01)

Edwards Syndrome: Family positive effects when life survival surpasses the expectation. Case report.
by: A. E. Chiaradia, et al.
Published: (2021-01-01)

Edward Syndrome with Aplasia Cutis Congenita: A Rare Case Report
by: Shubhankar Mishra, et al.
Published: (2014-07-01)

Rastreamento da síndrome de Down com uso de escore de múltiplos parâmetros ultra-sonográficos Ultrasound screening for Down syndrome using a multiparameter score
by: Victor Bunduki, et al.
Published: (1998-10-01)

The natural history of pregnancies with prenatal diagnosis of Trisomy 18 or Trisomy 13: Retrospective cases of a 23-year experience in a Brazilian public hospital
by: Julio Alejandro Peña Duque, et al.

Intrauterine death in singleton pregnancies with trisomy 21, 18, 13 and monosomy X
by: Vanessa Vigna Goulart, et al.
Published: (2016-04-01)

Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 15 at amniocentesis
by: Chih-Ping Chen, et al.
Published: (2020-09-01)

Mosaic trisomy 15 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review
by: Chih-Ping Chen, et al.
Published: (2015-08-01)

Mosaic trisomy 12 at amniocentesis: Prenatal diagnosis and molecular genetic analysis
by: Chih-Ping Chen, et al.
Published: (2013-03-01)

Síndrome de Edwards asociado a inmunodeficiencia combinada Edwards' syndrome associated to combined immunodeficiency
by: Vianed Marsán Suárez, et al.
Published: (2011-09-01)

Diagnóstico pré-natal das genodermatoses Prenatal diagnosis of genodermatoses
by: Maria Carolina de Abreu Sampaio, et al.
Published: (2007-08-01)

Unusual Longevity of Edwards Syndrome: A Case Report
by: Abbas Alshami, et al.
Published: (2020-12-01)

Long Survival of a Patient with Trisomy 18 and Dandy-Walker Syndrome
by: Leonardo Moura Ferreira de Souza, et al.
Published: (2019-07-01)

Myoclonic epilepsy of late onset in trisomy 21 Epilepsia mioclônica de início tardio na trissomia 21
by: Lm. Li, et al.
Published: (1995-12-01)

Mosaic trisomy 17 at amniocentesis: Prenatal diagnosis, molecular genetic analysis, and literature review
by: Chih-Ping Chen, et al.
Published: (2016-10-01)

Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome
by: Chih-Ping Chen, et al.
Published: (2017-04-01)

Mosaic trisomy 2 at amniocentesis: Prenatal diagnosis and molecular genetic analysis
by: Chih-Ping Chen, et al.
Published: (2012-12-01)

Hidronefrose de Diagnóstico Pré-Natal. Casuística do Serviço de Pediatria do Hospital de São Teotónio — Viseu *
by: Vítor Bastos, et al.
Published: (2014-09-01)

Isolated trisomy 11 in de novo acute myeloid leukemia Trissomia 11 isolada em leucemia mielóide aguda de novo
by: Everson A. Krum, et al.
Published: (2008-01-01)

Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism
by: Chih-Ping Chen, et al.
Published: (2013-09-01)

Prenatal diagnosis of maternal uniparental disomy 5 by amniocentesis associated with confined placental mosaicism for trisomy 5 and fetal trisomy 21 in a pregnancy
by: Chih-Ping Chen, et al.
Published: (2020-11-01)

Monochorionic twins discordant for trisomy 13: A case report, systematic literature search and synthesis of available evidence
by: Emily F. Cornish, et al.
Published: (2020-12-01)

Unbalanced and Balanced Acrocentric Rearrangements Involving Chromosomes Other Than Chromosome 21 at Amniocentesis
by: Chih-Ping Chen, et al.
Published: (2009-12-01)

Idade materna e síndrome de Down no Nordeste do Brasil Maternal age and Down syndrome in Northeast Brazil
by: Fábio A. F. Gusmão, et al.
Published: (2003-08-01)

Apresentações clínicas não usuais de pacientes portadores de síndrome de Patau e Edwards: um desafio diagnóstico? Unusual clinical presentations of patients with Patau and Edwards syndromes: a diagnostic challenge?
by: Paulo Ricardo G. Zen, et al.
Published: (2008-09-01)