Prenatal diagnosis of 7q11.23 duplication in a fetus with renal pelvic dilatation and the postnatal outcome

7q11.23 duplication syndrome is a multisystemic developmental disorder characterized by variable manifestations, such as speech delay, mild craniofacial anomalies with distinctive facial features, and intellectual ability ranging from mental retardation to normal cognitive development. Approximately...

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Detalhes bibliográficos
Autor principal: Serafim, S. (author)
Outros Autores: Ferreira, C. (author), Simão, L. (author), Alves, C. (author), Brito, F. (author), Silva, M. (author), Furtado, J. (author), Viegas, M. (author), Pedro, S. (author), Marques, B. (author), Rodrigues, M. (author), Sá, J. (author), Castro, M.J. (author), Mendes, P. (author), Vassal, H. (author), Correia, H. (author)
Formato: conferenceObject
Idioma:eng
Publicado em: 2019
Assuntos:
Prenatal Diagnosis
7q11.23 Duplication
Doenças Genéticas
Texto completo:http://hdl.handle.net/10400.18/5910
País:Portugal
Oai:oai:repositorio.insa.pt:10400.18/5910

Texto Completo

http://hdl.handle.net/10400.18/5910

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