K. Salameh, Rajai Al Bedaywi, N. Elkabir, R. Valappil, Anvar P. Vellamgot, L. Habboub
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引用次数: 1
摘要
简介:多肢症(多肢)或先天性肢体重复是一种极为罕见的人类疾病,文献报道的病例很少。病例报告:这是一例新生女性,出生时右腿多出尾巴状,不幸的是在常规产前超声检查中未被发现。结论:早期诊断有助于家长制定治疗计划,做好心理准备。对于多尿症患者,建议在早期手术切除副肢。*通信:Khalil Salameh, Al Wakra医院儿科和新生儿科,哈马德医疗公司,Al Wakra,卡塔尔,电话:+974 40114258。收稿日期:2020年11月4日;收稿日期:2020年11月25日儿科与新生儿杂志ISSN 2689-1085
Duplicate Tail Like Right Lower Limb: A Rare Congenital Malformation
Introduction: Polymelia (supernumerary limbs) or congenital duplication of limb is an extremely rare condition in humans, with only few cases reported in the literature. Case Report: This is a case of newborn female born with a tail-like extra right leg, which unfortunately was not detected during the routine antenatal ultrasonography. Conclusion: Early diagnosis can facilitate the management planning and psychological preparation of the parents. Surgical resection of the accessory limb at an early age is recommended in patients with polymelia. *Correspondence: Khalil Salameh, Department of Pediatrics and Neonatology, Al Wakra Hospital, Hamad Medical Corporation, Al Wakra, Qatar, Tel: +974 40114258. Received: 04 November 2020; Accepted: 25 November 2020 Journal of Pediatrics & Neonatology ISSN 2689-1085