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Ellis-van Creveld syndrome in an Indian child: a case report
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  • Ellis-van Creveld syndrome in an Indian child: a case report
  • Ellis-van Creveld syndrome in an Indian child: a case report
저자명
Veena. K.M.,Jagadishchandra. H.,Rao. Prasanna Kumar,Chatra. Laxmikanth
간행물명
Imaging science in dentistry
권/호정보
2011년|41권 4호|pp.167-170 (4 pages)
발행정보
대한구강악안면방사선학회
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정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

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.