Muhammed Khaled Al Hamad, Mohammad Abdullah Kokash, Samah Khirou Ismaeil, Abdulrahman Ahmad Othman, Raneem Alrehani, Hussein Fares Hussein, Bassam Abdul Muttalib ALHameed, Alhareth Hassan Alghabra, Baraa Mustafa Boulad, Eyas Issam Idrees, Bilal Sleiay, Mouhammed Sleiay
{"title":"A 17-year-old female with Down syndrome and Crohn's disease: a rare case report from Syria.","authors":"Muhammed Khaled Al Hamad, Mohammad Abdullah Kokash, Samah Khirou Ismaeil, Abdulrahman Ahmad Othman, Raneem Alrehani, Hussein Fares Hussein, Bassam Abdul Muttalib ALHameed, Alhareth Hassan Alghabra, Baraa Mustafa Boulad, Eyas Issam Idrees, Bilal Sleiay, Mouhammed Sleiay","doi":"10.1097/MS9.0000000000003627","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Down syndrome (DS) affects 1 in 787 live births, linked to congenital anomalies and intellectual impairment. Colorectal Crohn's disease is prevalent in DS patients, presenting with fatigue, abdominal pain, and strictures, often treated with surgery, immunomodulators, and biotherapy for management.</p><p><strong>Case presentation: </strong>The patient presented with symptoms of abdominal pain, cramping, and significant bowel sounds, along with weight loss and a decreased appetite. Histopathological examination and upper endoscopy were used to diagnose the condition, and a gluten-free dietary treatment was implemented.</p><p><strong>Clinical discussion: </strong>Crohn's disease can be diagnosed by several methods, including histopathology, and its treatment can involve various approaches, including dietary management. There is a connection with genetic diseases, and it is not necessary for all symptoms and signs of the disease to appear, as they often vary.</p><p><strong>Conclusion: </strong>DS with Crohn's disease is considered a very rare condition, especially in low-income countries and at a young age. It should be taken into account when differentiating diagnoses in autoimmune and intestinal diseases.</p>","PeriodicalId":8025,"journal":{"name":"Annals of Medicine and Surgery","volume":"87 9","pages":"6057-6060"},"PeriodicalIF":1.6000,"publicationDate":"2025-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12401191/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of Medicine and Surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1097/MS9.0000000000003627","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/9/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
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Abstract
Introduction: Down syndrome (DS) affects 1 in 787 live births, linked to congenital anomalies and intellectual impairment. Colorectal Crohn's disease is prevalent in DS patients, presenting with fatigue, abdominal pain, and strictures, often treated with surgery, immunomodulators, and biotherapy for management.
Case presentation: The patient presented with symptoms of abdominal pain, cramping, and significant bowel sounds, along with weight loss and a decreased appetite. Histopathological examination and upper endoscopy were used to diagnose the condition, and a gluten-free dietary treatment was implemented.
Clinical discussion: Crohn's disease can be diagnosed by several methods, including histopathology, and its treatment can involve various approaches, including dietary management. There is a connection with genetic diseases, and it is not necessary for all symptoms and signs of the disease to appear, as they often vary.
Conclusion: DS with Crohn's disease is considered a very rare condition, especially in low-income countries and at a young age. It should be taken into account when differentiating diagnoses in autoimmune and intestinal diseases.
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