Usefulness of Early Genetic Diagnosis for Twins With a Family History of Congenital Nephrotic Syndrome

We reported a dichorionic diamniotic placental twin (DD twin) with a family history of a congenital nephrotic syndrome of the Finnish type (CNF), of which the parent had heterozygous for the NPHS1 gene mutation. The DD twin was born at 36 weeks gestation, and their fused placenta weighed 1,340 g. Al...

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Detalles Bibliográficos
Autores principales: Toya, Yukiko, Ishikawa, Ken, Yoshida, Taro, Matsumoto, Atsushi, Akasaka, Manami, Nozu, Kandai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10124580/
https://www.ncbi.nlm.nih.gov/pubmed/37101999
http://dx.doi.org/10.7759/cureus.36667

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10124580/
https://www.ncbi.nlm.nih.gov/pubmed/37101999
http://dx.doi.org/10.7759/cureus.36667

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