Clinical analysis of monochorionic-diamniotic twins with genetic discordance / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 538-542, 2023.
Artigo
em Chinês
| WPRIM (Pacífico Ocidental)
| ID: wpr-981784
Biblioteca responsável:
WPRO
ABSTRACT
OBJECTIVE@#To explore the genetic etiology of 5 cases of monochorionic-diamniotic (MCDA) with genetic discordance.@*METHODS@#148 cases of MCDA twins who were diagnosed by amniocentesis at the Maternal and Child Health Care Hospital of Guangxi Zhuang Autonomous Region from January 2016 to June 2020 were selected as the study subjects. Relevant clinical data of the pregnant women were collected, and amniotic fluid samples of the twins were collected separately. Chromosomal karyotyping analysis and single nucleotide polymorphism array (SNP array) assay were carried out.@*RESULTS@#The results of chromosomal karyotyping analysis showed that 5 of the MCDA twins had inconsistent chromosome karyotypes, with an incidence of 3.4% (5/148). SNP array assay showed that 3 fetuses were mosaics.@*CONCLUSION@#Genetic discordance occurs among MCDA twins, and prenatal counseling for such cases should be given by doctors with experience in medical genetics and fetal medicine, and personalized clinical management should be recommended.
Texto completo:
Disponível
Base de dados:
WPRIM (Pacífico Ocidental)
Assunto principal:
Gêmeos
/
Gêmeos Monozigóticos
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China
/
Estudos Retrospectivos
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Ultrassonografia Pré-Natal
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Feto
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Amniocentese
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Cariotipagem
Limite:
Criança
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Feminino
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Humanos
/
Gravidez
País/Região como assunto:
Ásia
Idioma:
Chinês
Revista:
Chinese Journal of Medical Genetics
Ano de publicação:
2023
Tipo de documento:
Artigo