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Ellis-van Creveld syndrome in an Indian child: a case report

机译:一名印度儿童的Ellis-van Creveld综合征:一例病例报告

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摘要

Ellis-van Creveld syndrome is a rare congenital genetic disorder having autosomal recessive inheritance. It is a syndrome affecting the Amish population of Pennsylvania in USA with prevalence rate of 1/5,000 live at birth. In non-Amish population, the birth prevalence is 7/1,000,000. The syndrome is characterized by bilateral postaxial polydactyly of the hands, chondrodysplasia of long bones resulting in acromesomelic dwarfism, ectodermal dysplasia affecting nails as well as teeth and congenital heart malformation. There were very rare reports of this syndrome in dentistry. The present case focuses on the striking and constant oral findings of these patients, which are the main diagnostic features of this syndrome. Since the oral manifestations affect the esthetic, speech, and jaw growth of the child, the dentists have an important role to play in proper management of such case.
机译:Ellis-van Creveld综合征是一种罕见的先天性遗传疾病,具有常染色体隐性遗传。这是一种影响美国宾夕法尼亚州阿米什人人口的综合症,出生时的患病率为1 / 5,000。在非阿米什人中,出生率为7 / 1,000,000。该综合征的特征是手的双侧后轴多指,长骨头的软骨发育不良,导致顶体矮化,影响指甲的外胚层发育不良以及牙齿和先天性心脏畸形。牙科上很少有这种综合征的报道。本病例侧重于这些患者的惊人且持续的口腔检查结果,这是该综合征的主要诊断特征。由于口头表现会影响孩子的审美,言语和下颌生长,因此牙医在适当处理这种情况方面起着重要作用。

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