Delayed presentation of congenital rectal stenosis associated with Down's syndrome and hypothyroidism: Case report

Abstract Rectal stenosis is a rare variety of rectal atresia. A membrane separates the rectum from the anal canal in the presence of a normal anus. We report a case of rectal stenosis associated with Down's syndrome and hypothyroidism in whom rectal stenosis was diagnosed at the age of 17 years...

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Autores principales:	Tanvir Kabir Chowdhury, Md. Mozammel Hoque, Mahfuzul Kabir, Tahmina Banu
Formato:	article
Lenguaje:	EN
Publicado:	Wiley 2021
Materias:	case report Down's syndrome hypothyroidism rectal atresia rectal stenosis Medicine R Medicine (General) R5-920
Acceso en línea:	https://doaj.org/article/1cbfcf9c4f8d43c590dd5fd27b2e5aef
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spelling	oai:doaj.org-article:1cbfcf9c4f8d43c590dd5fd27b2e5aef2021-12-01T06:36:08ZDelayed presentation of congenital rectal stenosis associated with Down's syndrome and hypothyroidism: Case report2050-090410.1002/ccr3.5083https://doaj.org/article/1cbfcf9c4f8d43c590dd5fd27b2e5aef2021-11-01T00:00:00Zhttps://doi.org/10.1002/ccr3.5083https://doaj.org/toc/2050-0904Abstract Rectal stenosis is a rare variety of rectal atresia. A membrane separates the rectum from the anal canal in the presence of a normal anus. We report a case of rectal stenosis associated with Down's syndrome and hypothyroidism in whom rectal stenosis was diagnosed at the age of 17 years.Tanvir Kabir ChowdhuryMd. Mozammel HoqueMahfuzul KabirTahmina BanuWileyarticlecase reportDown's syndromehypothyroidismrectal atresiarectal stenosisMedicineRMedicine (General)R5-920ENClinical Case Reports, Vol 9, Iss 11, Pp n/a-n/a (2021)
institution	DOAJ
collection	DOAJ
language	EN
topic	case report Down's syndrome hypothyroidism rectal atresia rectal stenosis Medicine R Medicine (General) R5-920
spellingShingle	case report Down's syndrome hypothyroidism rectal atresia rectal stenosis Medicine R Medicine (General) R5-920 Tanvir Kabir Chowdhury Md. Mozammel Hoque Mahfuzul Kabir Tahmina Banu Delayed presentation of congenital rectal stenosis associated with Down's syndrome and hypothyroidism: Case report
description	Abstract Rectal stenosis is a rare variety of rectal atresia. A membrane separates the rectum from the anal canal in the presence of a normal anus. We report a case of rectal stenosis associated with Down's syndrome and hypothyroidism in whom rectal stenosis was diagnosed at the age of 17 years.
format	article
author	Tanvir Kabir Chowdhury Md. Mozammel Hoque Mahfuzul Kabir Tahmina Banu
author_facet	Tanvir Kabir Chowdhury Md. Mozammel Hoque Mahfuzul Kabir Tahmina Banu
author_sort	Tanvir Kabir Chowdhury
title	Delayed presentation of congenital rectal stenosis associated with Down's syndrome and hypothyroidism: Case report
title_short	Delayed presentation of congenital rectal stenosis associated with Down's syndrome and hypothyroidism: Case report
title_full	Delayed presentation of congenital rectal stenosis associated with Down's syndrome and hypothyroidism: Case report
title_fullStr	Delayed presentation of congenital rectal stenosis associated with Down's syndrome and hypothyroidism: Case report
title_full_unstemmed	Delayed presentation of congenital rectal stenosis associated with Down's syndrome and hypothyroidism: Case report
title_sort	delayed presentation of congenital rectal stenosis associated with down's syndrome and hypothyroidism: case report
publisher	Wiley
publishDate	2021
url	https://doaj.org/article/1cbfcf9c4f8d43c590dd5fd27b2e5aef
work_keys_str_mv	AT tanvirkabirchowdhury delayedpresentationofcongenitalrectalstenosisassociatedwithdownssyndromeandhypothyroidismcasereport AT mdmozammelhoque delayedpresentationofcongenitalrectalstenosisassociatedwithdownssyndromeandhypothyroidismcasereport AT mahfuzulkabir delayedpresentationofcongenitalrectalstenosisassociatedwithdownssyndromeandhypothyroidismcasereport AT tahminabanu delayedpresentationofcongenitalrectalstenosisassociatedwithdownssyndromeandhypothyroidismcasereport
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Delayed presentation of congenital rectal stenosis associated with Down's syndrome and hypothyroidism: Case report

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