Prenatal diagnosis of Lowe syndrome in a male fetus with isolated bilateral cataract.

Rouxel, Flavien; Fauré, Julien; Faure, Jean-Michel; Deschamps, Françoise; Burlet, Gilles; Flandrin, Anaig; Couture, Alain; Prodhomme, Olivier; Rendu, John; Willems, Marjolaine

Rouxel, Flavien; Fauré, Julien; Faure, Jean-Michel; Deschamps, Françoise; Burlet, Gilles; Flandrin, Anaig; Couture, Alain; Prodhomme, Olivier; Rendu, John; Willems, Marjolaine.

Afiliación

Rouxel F; Department of Medical Genetics, Rare Diseases and Personalized Medicine, Reference Center AD SOOR, AnDDI-RARE, Montpellier University, Centre Hospitalier Montpellier, 34090 Montpellier, France.
Fauré J; Univ. Grenoble Alpes, Inserm, U1216, CHU Grenoble Alpes, GIN, France.
Faure JM; Departement of obstetrics and gynecology, CHRU Montpellier, France.
Deschamps F; Departement of obstetrics and gynecology, CHRU Montpellier, France.
Burlet G; Departement of obstetrics and gynecology, CHRU Montpellier, France.
Flandrin A; Departement of obstetrics and gynecology, CHRU Montpellier, France.
Couture A; Department of Pediatric Radiology, CHRU Montpellier, France.
Prodhomme O; Department of Pediatric Radiology, CHRU Montpellier, France.
Rendu J; Univ. Grenoble Alpes, Inserm, U1216, CHU Grenoble Alpes, GIN, France.
Willems M; Department of Medical Genetics, Rare Diseases and Personalized Medicine, Reference Center AD SOOR, AnDDI-RARE, Montpellier University, Centre Hospitalier Montpellier, 34090 Montpellier, France.

Heliyon ; 8(12): e12210, 2022 Dec.

Article en En | MEDLINE | ID: mdl-36568675

Palabras clave

Fetus; Isolated cataract; Lowe syndrome; OCRL; X-linked

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Heliyon Año: 2022 Tipo del documento: Article País de afiliación: Francia

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