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Guidelines for NGS procedures applied to prenatal diagnosis by the Spanish Society of Gynecology and Obstetrics and the Spanish Association of Prenatal Diagnosis.
Abulí, Anna; Antolín, Eugenia; Borrell, Antoni; Garcia-Hoyos, Maria; García Santiago, Fe; Gómez Manjón, Irene; Maíz, Nerea; González González, Cristina; Rodríguez-Revenga, Laia; Valenzuena Palafoll, Irene; Suela, Javier.
Affiliation
  • Abulí A; Clinical and Molecular Genetics, Vall d'Hebron University Hospital, Barcelona, Spain.
  • Antolín E; Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.
  • Borrell A; Gynecology and Obstetrics, La Paz University Hospital, Madrid, Spain.
  • Garcia-Hoyos M; Gynecology and Obstetrics, Clinic Hospital of Barcelona, Barcelona, Spain.
  • García Santiago F; NIMGenetics Laboratory, Madrid, Spain.
  • Gómez Manjón I; Genetics, La Paz University Hospital, Madrid, Spain.
  • Maíz N; Genetics, Doce de Octubre University Hospital, Madrid, Spain.
  • González González C; Maternal-Fetal Medicine Research Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.
  • Rodríguez-Revenga L; Obstetrics, Vall d'Hebron University Hospital, Barcelona, Spain.
  • Valenzuena Palafoll I; Genetics, Infanta Sofía University Hospital, San Sebastian de los Reyes, Madrid, Spain.
  • Suela J; Biochemistry and Molecular Genetics, Clinic Hospital of Barcelona, Barcelona, Spain.
J Med Genet ; 61(8): 727-733, 2024 Jul 19.
Article in En | MEDLINE | ID: mdl-38834294
ABSTRACT

OBJECTIVE:

This document addresses the clinical application of next-generation sequencing (NGS) technologies for prenatal genetic diagnosis and aims to establish clinical practice recommendations in Spain to ensure uniformity in implementing these technologies into prenatal care.

METHODS:

A joint committee of expert obstetricians and geneticists was created to review the existing literature on fetal NGS for genetic diagnosis and to make recommendations for Spanish healthcare professionals.

RESULTS:

This guideline summarises technical aspects of NGS technologies, clinical indications in prenatal setting, considerations regarding findings to be reported, genetic counselling considerations as well as data storage and protection policies.

CONCLUSIONS:

This document provides updated recommendations for the use of NGS diagnostic tests in prenatal diagnosis. These recommendations should be periodically reviewed as our knowledge of the clinical utility of NGS technologies, applied during pregnancy, may advance.
Subject(s)
Key words

Full text: 1 Database: MEDLINE Main subject: Prenatal Diagnosis / High-Throughput Nucleotide Sequencing Limits: Female / Humans / Pregnancy Country/Region as subject: Europa Language: En Journal: J Med Genet Year: 2024 Type: Article Affiliation country: Spain

Full text: 1 Database: MEDLINE Main subject: Prenatal Diagnosis / High-Throughput Nucleotide Sequencing Limits: Female / Humans / Pregnancy Country/Region as subject: Europa Language: En Journal: J Med Genet Year: 2024 Type: Article Affiliation country: Spain