Caudal Regression Syndrome— a rare congenital disorder: a case report
Abstract Caudal regression syndrome is a rare anomaly that is characterised by impaired development of the lower half of the body. This includes absent or abnormal development of lumbar and sacrococcygeal segments. Other associations of this disease include abnormalities of genitourinary tract, g...
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Format: | Article |
Language: | English |
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Pakistan Medical Association
2022-01-01
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Series: | Journal of the Pakistan Medical Association |
Online Access: | https://www.ojs.jpma.org.pk/index.php/public_html/article/view/499 |
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author | Syed Muslim Mehdi Usman Baig Muhammad Hamza Zia Nosheen Iftikhar |
author_facet | Syed Muslim Mehdi Usman Baig Muhammad Hamza Zia Nosheen Iftikhar |
author_sort | Syed Muslim Mehdi |
collection | DOAJ |
description |
Abstract
Caudal regression syndrome is a rare anomaly that is characterised by impaired development of the lower half of the body. This includes absent or abnormal development of lumbar and sacrococcygeal segments. Other associations of this disease include abnormalities of genitourinary tract, gastrointestinal tract, and cardiopulmonary system. The exact aetiology is unknown and is believed to be multifactorial but maternal diabetes is significantly linked to this rare disorder. We report the case of a new-born baby boy with caudal regression syndrome, hyperbilirubinaemia and patent ductus arteriosus.
Keywords: Caudal Regression syndrome (CRS), Caudal Dysplasia, Sacral Agenesis, Patent Ductus Arteriosus (PDA)
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first_indexed | 2024-03-13T09:43:46Z |
format | Article |
id | doaj.art-a8b91a81aced4bcea25e15ee615ec396 |
institution | Directory Open Access Journal |
issn | 0030-9982 |
language | English |
last_indexed | 2024-03-13T09:43:46Z |
publishDate | 2022-01-01 |
publisher | Pakistan Medical Association |
record_format | Article |
series | Journal of the Pakistan Medical Association |
spelling | doaj.art-a8b91a81aced4bcea25e15ee615ec3962023-05-25T04:23:25ZengPakistan Medical AssociationJournal of the Pakistan Medical Association0030-99822022-01-01711210.47391/JPMA.01-499Caudal Regression Syndrome— a rare congenital disorder: a case reportSyed Muslim Mehdi 0Usman Baig 1Muhammad Hamza Zia 2Nosheen Iftikhar 3Final Year MBBS Student, Sharif Medical and Dental College, Lahore, PakistanFinal Year MBBS Student, Sharif Medical and Dental College, Lahore, PakistanFinal Year MBBS Student, Sharif Medical and Dental College, Lahore, PakistanDepartment of Pediatrics, Sharif Medical and Dental College, Lahore, Pakistan Abstract Caudal regression syndrome is a rare anomaly that is characterised by impaired development of the lower half of the body. This includes absent or abnormal development of lumbar and sacrococcygeal segments. Other associations of this disease include abnormalities of genitourinary tract, gastrointestinal tract, and cardiopulmonary system. The exact aetiology is unknown and is believed to be multifactorial but maternal diabetes is significantly linked to this rare disorder. We report the case of a new-born baby boy with caudal regression syndrome, hyperbilirubinaemia and patent ductus arteriosus. Keywords: Caudal Regression syndrome (CRS), Caudal Dysplasia, Sacral Agenesis, Patent Ductus Arteriosus (PDA) https://www.ojs.jpma.org.pk/index.php/public_html/article/view/499 |
spellingShingle | Syed Muslim Mehdi Usman Baig Muhammad Hamza Zia Nosheen Iftikhar Caudal Regression Syndrome— a rare congenital disorder: a case report Journal of the Pakistan Medical Association |
title | Caudal Regression Syndrome— a rare congenital disorder: a case report |
title_full | Caudal Regression Syndrome— a rare congenital disorder: a case report |
title_fullStr | Caudal Regression Syndrome— a rare congenital disorder: a case report |
title_full_unstemmed | Caudal Regression Syndrome— a rare congenital disorder: a case report |
title_short | Caudal Regression Syndrome— a rare congenital disorder: a case report |
title_sort | caudal regression syndrome a rare congenital disorder a case report |
url | https://www.ojs.jpma.org.pk/index.php/public_html/article/view/499 |
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