Popliteal Pterygium Syndrome (Facio-Genito-Popliteal Syndrome)

N. Mariappan, S. Shetty
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引用次数: 3

Abstract

Background: IRF6-related disorders span a spectrum from isolated cleft lip and palate and Van der Woude syndrome (VWS) at the mild end to popliteal pterygium syndrome (PPS) at the more severe end. Popliteal pterygia are found in popliteal pterygium syndrome, multiple pterygium syndrome and Arthrogryposis. The popliteal pterygium syndrome is a rare congenital condition, in which the patient has facial, genitourinary and skeletal anomalies along with popliteal pterygium. Autosomal dominant popliteal pterygium syndrome (AD-PPS) is a rare genetic malformation disorder characterized by cleft lip, with or without cleft palate, contractures of the lower extremities, abnormal external genitalia, syndactyly of fingers and/or toes, and a pyramidal skin fold over the hallux nail. AD-PPS is associated with mutations in the IRF6 gene (1q32.2-q32.3), involved in the formation of connective and epithelial tissues. Almost all affected patients harbor mutations in this gene. The word ‘pterygium’ is derived from the Greek word pterygion, which means wing. Pathologically it denotes a wing-like abnormal band of tissue. The most obvious characteristics of this syndrome are popliteal pterygium and a triangular crease of skin over the hallux. The orofacial findings include cleft lip, cleft palate, lower lip pits, a few missing teeth, and severely decayed teeth. The dental problems are overshadowed by the major syndromic manifestations. These patients have special dental needs and early preventive dental care and appropriate dental treatment at the optimal time is important. Diagnosis of pterygium syndrome is based on the clinical findings and confirmed by molecular genetic testing. AD-PPS is highly associated with missense mutations that alter residues that are predicted to interact directly with DNA in exons 3 and 4 of IRF6. Conclusion: An understanding of the molecular genetic basis of this syndrome is essential for prenatal diagnosis and also for genetic counseling of the parents. Keywords: Popliteal pterygium syndrome, Escobar syndrome, Magnetic resonance imaging, Congenital contractures, Genetic counseling.
腘窝翼状胬肉综合征(面部-生殖-腘窝综合征)
背景:irf6相关疾病的范围广泛,从轻度的孤立性唇腭裂和Van der Woude综合征(VWS)到较严重的腘侧翼状胬肉综合征(PPS)。翼状胬肉见于翼状胬肉综合征、多发性翼状胬肉综合征和关节挛缩症。腘窝翼状胬肉综合征是一种罕见的先天性疾病,患者在腘窝翼状胬肉的同时伴有面部、泌尿生殖系统和骨骼异常。常染色体显性腘翼状胬肉综合征(AD-PPS)是一种罕见的遗传畸形疾病,其特征是唇裂,伴或不伴腭裂,下肢挛缩,外生殖器异常,手指和/或脚趾并指,拇甲上锥体状皮肤褶皱。AD-PPS与IRF6基因(1q32.2-q32.3)突变有关,参与结缔组织和上皮组织的形成。几乎所有受影响的患者都携带这种基因突变。“pterygium”这个词来源于希腊语“pterygion”,意思是“翅膀”。病理上它表示一个翅膀状的异常组织带。这种综合征最明显的特征是腘窝翼状胬肉和拇上的三角形皮肤皱褶。口腔面部表现包括唇裂、腭裂、下唇凹陷、少量缺牙和严重蛀牙。主要的症状表现掩盖了牙齿问题。这些病人有特殊的牙科需要,及早进行预防性牙科护理,并在最佳时间接受适当的牙科治疗,是非常重要的。翼状胬肉综合征的诊断是基于临床表现和分子基因检测的证实。AD-PPS与误义突变高度相关,误义突变改变了IRF6外显子3和4中预测与DNA直接相互作用的残基。结论:了解该综合征的分子遗传学基础对产前诊断和家长遗传咨询具有重要意义。关键词:腘窝翼状胬肉综合征,Escobar综合征,磁共振成像,先天性挛缩,遗传咨询
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