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Prenatal diagnosis of cystinuria with a heterozygous pathogenic variant in SLC7A9 gene associated with isolated hyperechogenic fetal kidneys: A case report.
Aigbogun, Osaretin Pamela; Vancoppenolle, Noémie; Coppens, Sandra; Marangoni, Martina; Elsen, Elodie; Cassart, Marie; Gounongbe, Caroline.
Afiliação
  • Aigbogun OP; Department of Fetal Medicine CHU Saint Pierre Brussels Belgium.
  • Vancoppenolle N; Department of Fetal Medicine CHU Saint Pierre Brussels Belgium.
  • Coppens S; ULB Center of Human Genetics, Hôpital Universitaire de Bruxelles, Université Libre de Bruxelles Brussels Belgium.
  • Marangoni M; ULB Center of Human Genetics, Hôpital Universitaire de Bruxelles, Université Libre de Bruxelles Brussels Belgium.
  • Elsen E; Department of Fetal Medicine CHU Saint Pierre Brussels Belgium.
  • Cassart M; Department of Fetal Medicine CHU Saint Pierre Brussels Belgium.
  • Gounongbe C; Department of Radiology and Fetal Medicine Iris Sud Hospitals Brussels Belgium.
Clin Case Rep ; 12(7): e8730, 2024 Jul.
Article em En | MEDLINE | ID: mdl-39015212
ABSTRACT
Cystinuria is suspected antenatally by a hyperechogenic fetal colonic content. We report the first prenatal case of autosomal dominant SLC7A9-related cystinuria associated with isolated hyperechogenic kidneys as the only prenatal sonographic sign.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article