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X连锁低磷血症青少年和成人的中足和前足疾病

Midfoot and Forefoot Disorders in Adolescents and Adults with X-Linked Hypophosphatemia.

作者信息

Wenzel-Schwarz Florian, Akta Celine C, Stauffer Alexandra, Raimann Adalbert, Kocijan Roland, Ganger Rudolf, Mindler Gabriel T

机构信息

Department of Pediatric Orthopaedics and Foot Surgery, Orthopaedic Hospital Speising, Speisinger Strasse 109, 1130 Vienna, Austria.

Vienna Bone and Growth Center, Währinger Gürtel 18-20, 1090 Vienna, Austria.

出版信息

J Clin Med. 2024 Nov 9;13(22):6749. doi: 10.3390/jcm13226749.

Abstract

: X-linked hypophosphatemia (XLH, OMIM 307800) is a rare genetic disorder that affects phosphate metabolism. While lower limb deformity represents a hallmark symptom of patients with XLH, the effect on the foot has not been investigated. This study aimed to characterise foot pathologies and assess related outcome scores in adolescents and adults with XLH. : Patients aged ≥ 16 years with genetically verified XLH were included in this study. Physical examination was performed, and foot scores as well as foot X-rays were assessed. Radiographic analysis included the assessment of osteoarthritis, enthesopathies, and alignment abnormalities. : Twenty-six participants (51 limbs) with a mean age of 33.9 ± 15.4 years were eligible for the study. Patients with XLH presented with flatfoot deformity (reduced Meary angles > -4° in 84.3%), elevated first and fifth metatarsal angles > 30° (IM 1-5, 53.5%) and hallux valgus angles > 15° (36.0%). Moderate-to-severe joint space narrowing was observed in the talonavicular (49%) and cuneonavicular joints (41.2%). The American Orthopedic Foot and Ankle Society (AOFAS) score was associated with mildly reduced midfoot function. : A high rate of bony deformity, joint degeneration, and decreased foot scores indicated the impact of forefoot and midfoot disorders in patients with XLH.

摘要

X连锁低磷血症(XLH,OMIM 307800)是一种影响磷代谢的罕见遗传性疾病。虽然下肢畸形是XLH患者的标志性症状,但对足部的影响尚未得到研究。本研究旨在描述XLH青少年和成人的足部病变特征并评估相关结局评分。:本研究纳入了年龄≥16岁且经基因验证为XLH的患者。进行了体格检查,并评估了足部评分和足部X线片。影像学分析包括骨关节炎、附着点病和对线异常的评估。:26名平均年龄为33.9±15.4岁的参与者(51条肢体)符合研究条件。XLH患者表现为扁平足畸形(84.3%的患者Meary角减小>-4°)、第一和第五跖骨角升高>30°(IM 1-5,53.5%)以及拇外翻角>15°(36.0%)。距舟关节(49%)和楔舟关节(41.2%)观察到中度至重度关节间隙变窄。美国矫形足踝协会(AOFAS)评分与中足功能轻度降低相关。:高比例的骨畸形、关节退变和足部评分降低表明前足和中足疾病对XLH患者的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3526/11594587/641047c112d7/jcm-13-06749-g001.jpg

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