Congenital Hepatic Cyst in Patients With Patau Syndrome: A Rare Clinical Finding

Trisomy 13 (T13), frequently referred to as Patau syndrome, is a rare autosomal aneuploidy most commonly due to nondisjunction in meiosis. Frequently seen characteristics include cleft lip, cleft palate, cerebral defects, anophthalmia, and polydactyly among many more. We report a rare case of a newb...

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Detalles Bibliográficos
Autores principales: Rennick, Andrew C, Cardoso, Osmay, Saigal, Khushi, Boateng, Joseph, Saigal, Gaurav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Pediatric Surgery
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10620062/
https://www.ncbi.nlm.nih.gov/pubmed/37927679
http://dx.doi.org/10.7759/cureus.46377

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10620062/
https://www.ncbi.nlm.nih.gov/pubmed/37927679
http://dx.doi.org/10.7759/cureus.46377

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