科研速览 · Science Skim继续刷下去 · Keep skimming →
◆ Journal of general and family medicine2026-09-01

Late Recognition of Suspected Ehlers-Danlos Syndrome After Recurrent Small-Bowel Perforations: A Case Report.

Norio Horiguchi, Etsuko Hisanaga, Hiroko Sato, Kuniko Yoshida, Akihito Kimura, Ayumi Ito, Miki Horita, Aya Suzuki, Keiko Kawai-Kowase

一句话结论 · In one sentence

The overall phenotype supported clinically suspected EDS, but molecular confirmation was required for definitive subtype assignment.

原始摘要(英文原文)· Original abstract
BACKGROUND: Ehlers-Danlos syndrome (EDS) may be overlooked when gastrointestinal and musculoskeletal findings are assessed separately. CASE PRESENTATION: An older woman with two previous small-bowel perforations had bilateral congenital hip dislocation, recurrent shoulder dislocations, skin hyperextensibility, and muscularis propria thinning in nonperforated jejunum. Systematic reassessment using the 2017 classification met minimal clinical criteria suggestive of arthrochalasia EDS, while recurrent bowel perforation raised concern for vascular EDS. Genetic testing was declined. CONCLUSION: The overall phenotype supported clinically suspected EDS, but molecular confirmation was required for definitive subtype assignment.
读原文 · Read the paper ↗

AI 追问PRO

登录后使用 AI 追问

讨论区

登录后参与讨论

相关论文 · Related

Late Recognition of Suspected Ehlers-Danlos Syndrome After Recurrent Small-Bowel Perforations: A Case Report. — 科研速览 Science Skim