Two Pregnancies with a Different Outcome in a Patient with Alport Syndrome

BACKGROUND: Alport syndrome is a genetic disease that progresses to chronic kidney failure, with X-linked, autosomal dominant or autosomal recessive type of inheritance. Women are generally carriers of the mutation and have a milder form of the disease. During pregnancy, they have an increased risk...

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Detalles Bibliográficos
Autores principales: Kitanovska, Biljana Gerasimovska, Gerasimovska, Vesna, Livrinova, Vesna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Institute of Immunobiology and Human Genetics 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5042630/
https://www.ncbi.nlm.nih.gov/pubmed/27703570
http://dx.doi.org/10.3889/oamjms.2016.073

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5042630/
https://www.ncbi.nlm.nih.gov/pubmed/27703570
http://dx.doi.org/10.3889/oamjms.2016.073

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