Gastrointestinal complaints in patients with osteogenesis imperfecta: The bright side of a rare genetic disorder

Osteogenesis imperfecta (OI) is a rare hereditary disorder of connective tissue. A Danish national registry study surprisingly identified digestive causes as one of the leading causes of OI mortality. However, there is a dearth of prospective data describing gastrointestinal symptoms in OI. Our aim...

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Vydáno v:	Bone (New York, N.Y.) Ročník 200; s. 117589
Hlavní autoři:	Sharma, Disha, Viana Rodriguez, Gracia M., Lai, Chunwei Walter, Asif, Bilal, Talvacchio, Sara, Yang, Alexander H., Vittal, Anusha, Derkyi, Alberta, Koh, Christopher, Wright, Elizabeth C., Marini, Joan C., Heller, Theo
Médium:	Journal Article
Jazyk:	angličtina
Vydáno:	United States Elsevier Inc 01.11.2025
Témata:	Abdominal pain Adolescent Adult Constipation Female Gastrointestinal Gastrointestinal Diseases - complications Gastrointestinal Diseases - genetics Humans Male Motility Osteogenesis imperfecta Osteogenesis Imperfecta - complications Osteogenesis Imperfecta - genetics Prospective Studies Rare Diseases - genetics Skeletal dysplasia Surveys and Questionnaires Young Adult AR GI AD Motility NSAIDs Osteogenesis imperfecta Abdominal pain OI Skeletal dysplasia Gastrointestinal Constipation BMI
ISSN:	8756-3282, 1873-2763, 1873-2763
On-line přístup:	Získat plný text
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