Missed diagnosis of lissencephaly after prenatal diagnosis: A case report.

Liu, Mengna; Liu, Xiao; Wu, Jiebin; Sha, Jing; Zhai, Jingfang; Zhang, Bei

Liu, Mengna; Liu, Xiao; Wu, Jiebin; Sha, Jing; Zhai, Jingfang; Zhang, Bei.

Afiliación

Liu M; Department of Prenatal Diagnosis Medical Center, Xuzhou Central Hospital, Xuzhou Clinical School of Xuzhou Medical University, Xuzhou, Jiangsu, China.
Liu X; Department of Pediatrics, Xuzhou Central Hospital, Xuzhou Clinical School of Xuzhou Medical University, Xuzhou, Jiangsu, China.
Wu J; Department of Pediatrics, Xuzhou Central Hospital, Xuzhou Clinical School of Xuzhou Medical University, Xuzhou, Jiangsu, China.
Sha J; Department of Prenatal Diagnosis Medical Center, Xuzhou Central Hospital, Xuzhou Clinical School of Xuzhou Medical University, Xuzhou, Jiangsu, China.
Zhai J; Department of Prenatal Diagnosis Medical Center, Xuzhou Central Hospital, Xuzhou Clinical School of Xuzhou Medical University, Xuzhou, Jiangsu, China.
Zhang B; Key Laboratory of Brain Diseases Bioinformation of Xuzhou Medical University, Xuzhou, Jiangsu, China.

Medicine (Baltimore) ; 102(7): e33014, 2023 Feb 17.

Article en En | MEDLINE | ID: mdl-36800618

Asunto(s)

Variaciones en el Número de Copia de ADN; Lisencefalia; Lactante; Embarazo; Femenino; Humanos; Masculino; Diagnóstico Erróneo; Lisencefalia/diagnóstico; Lisencefalia/genética; Encéfalo; Diagnóstico Prenatal/métodos; Convulsiones; 1-Alquil-2-acetilglicerofosfocolina Esterasa/genética

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Lisencefalia / Variaciones en el Número de Copia de ADN Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans / Infant / Male / Pregnancy Idioma: En Revista: Medicine (Baltimore) Año: 2023 Tipo del documento: Article País de afiliación: China

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