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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2023
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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. |
format | Online Article Text |
id | pubmed-10620062 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
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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