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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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Autores principales: Rennick, Andrew C, Cardoso, Osmay, Saigal, Khushi, Boateng, Joseph, Saigal, Gaurav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
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
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author Rennick, Andrew C
Cardoso, Osmay
Saigal, Khushi
Boateng, Joseph
Saigal, Gaurav
author_facet Rennick, Andrew C
Cardoso, Osmay
Saigal, Khushi
Boateng, Joseph
Saigal, Gaurav
author_sort Rennick, Andrew C
collection PubMed
description 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 newborn female with T13, demonstrating several known anomalies associated with the syndrome and an associated large congenital hepatic cyst, exhibiting a significant mass effect on vital organs. Based on a literature review conducted in August 2023, we found no previous documentation of a congenital hepatic cyst reported with T13.
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spelling pubmed-106200622023-11-03 Congenital Hepatic Cyst in Patients With Patau Syndrome: A Rare Clinical Finding Rennick, Andrew C Cardoso, Osmay Saigal, Khushi Boateng, Joseph Saigal, Gaurav Cureus Pediatric Surgery 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 newborn female with T13, demonstrating several known anomalies associated with the syndrome and an associated large congenital hepatic cyst, exhibiting a significant mass effect on vital organs. Based on a literature review conducted in August 2023, we found no previous documentation of a congenital hepatic cyst reported with T13. Cureus 2023-10-02 /pmc/articles/PMC10620062/ /pubmed/37927679 http://dx.doi.org/10.7759/cureus.46377 Text en Copyright © 2023, Rennick et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Pediatric Surgery
Rennick, Andrew C
Cardoso, Osmay
Saigal, Khushi
Boateng, Joseph
Saigal, Gaurav
Congenital Hepatic Cyst in Patients With Patau Syndrome: A Rare Clinical Finding
title Congenital Hepatic Cyst in Patients With Patau Syndrome: A Rare Clinical Finding
title_full Congenital Hepatic Cyst in Patients With Patau Syndrome: A Rare Clinical Finding
title_fullStr Congenital Hepatic Cyst in Patients With Patau Syndrome: A Rare Clinical Finding
title_full_unstemmed Congenital Hepatic Cyst in Patients With Patau Syndrome: A Rare Clinical Finding
title_short Congenital Hepatic Cyst in Patients With Patau Syndrome: A Rare Clinical Finding
title_sort congenital hepatic cyst in patients with patau syndrome: a rare clinical finding
topic Pediatric Surgery
url 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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