Veena K M, Jagadishchandra H, Rao Prasanna Kumar, Chatra Laxmikanth
Department of Oral Medicine and Radiology, Yenepoya Dental College, Yenepoya University, Mangalore, India.
Imaging Sci Dent. 2011 Dec;41(4):167-70. doi: 10.5624/isd.2011.41.4.167. Epub 2011 Dec 19.
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.
埃利斯-范克里维尔德综合征是一种罕见的常染色体隐性遗传先天性疾病。它是一种影响美国宾夕法尼亚州阿米什人群的综合征,出生时患病率为1/5000。在非阿米什人群中,出生患病率为7/1000000。该综合征的特征包括双手双侧轴后多指畸形、长骨软骨发育不良导致肢端短侏儒症、影响指甲和牙齿的外胚层发育不良以及先天性心脏畸形。牙科领域关于该综合征的报道非常罕见。本病例重点关注这些患者显著且持续存在的口腔表现,这些表现是该综合征的主要诊断特征。由于口腔表现会影响儿童的美观、言语和颌骨发育,牙医在妥善管理此类病例中发挥着重要作用。