ACVR1中p.a g258gly伴进行性骨化性纤维发育不良严重变异异位骨化的快速进展:1例病例报告及临床表型回顾

Case Reports in Genetics Pub Date : 2022-08-25 eCollection Date: 2022-01-01 DOI:10.1155/2022/5021758
Kosei Hasegawa, Hiroyuki Tanaka, Natsuko Futagawa, Hiroyuki Miyahara, Hirokazu Tsukahara
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摘要

进行性骨化纤维发育不良(FOP)是一种罕见的骨骼疾病,其特征是先天性大脚趾畸形和进行性异位骨化。大脚趾畸形出现在出生时,而异位骨化通常发生在儿童时期,很少发生在婴儿期。经典的FOP来自ACVR1基因的杂合p.a g206his变体,该变体编码激活素A受体1型。近年来,一些非典型FOP患者出现了其他ACVR1基因变异,其临床特征在经典FOP患者中没有观察到。在这里,我们描述了一个女孩严重的FOP和多种异常,包括手和脚的并指,指甲发育不全,下颌骨发育不全,从婴儿期发生的异位骨化和先天性心脏畸形。在我们的患者中,我们发现了ACVR1的杂合p.a g258gly变异的新发生,此前仅在两例严重的FOP患者中报道过。与典型的FOP患者相比,异位骨化发生得更早、更频繁。我们报告了该患者异位骨化的时间序列变化,并将其临床特征与先前报道的p.a g258gly患者的临床特征进行了比较。我们的报告加深了对伴p.Arg258Gly的严重FOP临床特征和FOP作为一种全身性疾病的认识。
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Rapid Progression of Heterotopic Ossification in Severe Variant of Fibrodysplasia Ossificans Progressiva with p.Arg258Gly in ACVR1: A Case Report and Review of Clinical Phenotypes.

Fibrodysplasia ossificans progressiva (FOP) is a rare skeletal disorder characterized by congenital malformation of the great toes and progressive heterotopic ossification. Malformation of the great toes appears at birth, while heterotopic ossification generally occurs during childhood and rarely occurs during infancy. Classical FOP results from the heterozygous p.Arg206His variant of the ACVR1 gene, which encodes Activin A receptor type 1. Recently, some atypical FOP patients with other ACVR1 gene variants and clinical features that are not observed in classical FOP patients have been reported. Herein, we describe a girl with severe FOP and multiple anomalies, including syndactyly of the hands and feet, nail agenesis, mandibular hypoplasia, heterotopic ossification occurring from infancy, and congenital cardiac malformation. In our patient, we identified de novo occurrence of the heterozygous p.Arg258Gly variant of ACVR1, which has previously been reported in only two severe FOP patients. Heterotopic ossification occurred earlier and more frequently compared with classical FOP patients. We present the time-series changes in heterotopic ossification in our patient and compare her clinical features with those of the previously reported patients with p.Arg258Gly. Our report deepens understanding of the clinical features in severe FOP with p.Arg258Gly and of FOP as a systemic disorder.

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