Fibrodysplasia Ossificans Progressiva: A Case Report with Pseudo-Ankylosis of the Temporomandibular Joint.

IF 1.2 4区 医学 Q3 DENTISTRY, ORAL SURGERY & MEDICINE
Cleft Palate-Craniofacial Journal Pub Date : 2024-05-01 Epub Date: 2022-12-19 DOI:10.1177/10556656221146598
Sarut Chaisrisawadisuk, Kelly J Oliver, Sarah Constantine, Jonathan Azzopardi, Peter J Anderson, Mark H Moore
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引用次数: 0

Abstract

Fibrodysplasia ossificans progressiva (FOP) is a rare condition characterized by progressive heterotopic ossifications and congenital hallux valgus deformities. The common underlying genetic cause is an ACVR1 mutation, resulting in altered bone morphogenetic protein (BMP) regulation. Trauma and/or minor procedures aggravate the abnormal bony formation in soft tissues. This report presents a 3-year-old child with this condition who presented pseudo-ankylosis of the temporomandibular joint (TMJ) after minor craniofacial trauma. Abnormal ossification in the medial pterygoid muscle was identified as the causative abnormality for the presentation with trismus.

纤维增生性骨质疏松症:颞下颌关节假性强直的病例报告》(Fibrodysplasia Ossificans Progressiva: A Case Report with Pseudo-Ankylosis of Temporomandibular Joint)。
渐进性骨化性纤维增生症(FOP)是一种罕见疾病,以渐进性异位骨化和先天性拇指外翻畸形为特征。常见的潜在遗传原因是 ACVR1 基因突变,导致骨形态发生蛋白(BMP)调节发生改变。外伤和/或小手术会加重软组织中骨质的异常形成。本报告介绍了一名患有此病的 3 岁儿童,他在轻微颅面部创伤后出现颞下颌关节(TMJ)假性强直。经鉴定,翼内侧肌的异常骨化是导致患儿出现三趾畸形的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.70
自引率
36.40%
发文量
215
期刊介绍: The Cleft Palate-Craniofacial Journal (CPCJ) is the premiere peer-reviewed, interdisciplinary, international journal dedicated to current research on etiology, prevention, diagnosis, and treatment in all areas pertaining to craniofacial anomalies. CPCJ reports on basic science and clinical research aimed at better elucidating the pathogenesis, pathology, and optimal methods of treatment of cleft and craniofacial anomalies. The journal strives to foster communication and cooperation among professionals from all specialties.
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