P44.19: Sequential ultrasound examination for diagnosis of chondroectodermal dysplasia: Ellis-van Creveld Syndrome

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Chondroectodermal dysplasia (Ellis-Van Creveld syndrome: A case report

Ellis-Van Creveld syndrome is a very rare congenital disorder which its principal features are polysyndactyly, chondrodysplasia, cardiac abnormalities and ectodermal dysplasia. We report a 10-year-old girl with major manifestations of this syndrome who also had multiple brownish macules and patches on trunk and extremities with aortic and pulmonary stenosis in echocardiographic evaluations.

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Chondroectodermal dysplasia (Ellis-van Creveld syndrome): a case report.

Ellis-van Creveld (EVC) syndrome is a form of skeletal and chondroectodermal dysplasia, occurring with and without systemic involvement. Taurodontism of permanent and primary molars and upper posterior supernumerary teeth are rarely associated with this syndrome. A 5-year-old girl presented with early childhood caries and hypodontia. She had labiogingival adhesion, labiogingival frenulum hypert...

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Chondroectodermal dysplasia (Ellis-van Creveld syndrome): a case report

A case of chondroectodermal dysplasia (Ellis-van Creveld syndrome) with a remarkable number of the classic oral and dental changes is described. This syndrome involves all embryonic tissue layers and is polysymptomatic; yet some oral and dental manifestations are pathognomonic and must be considered in primary diagnostic criteria. However, in some patients, these oral and dental manifestations ...

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Ellis-van Creveld syndrome, (chondroectodermal dysplasia syndrome) in a Gurkha family.

The first reported case of Ellis--van Creveld syndrome in a Gurkha child is described, and the implications of the syndrome in this ethnic group are briefly considered.

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Ellis-van Creveld Syndrome.

A 21 years old male with typical features of Ellis-Van Creveld Syndrome is presented for its rarity. This is the second living case being reported from India.

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ژورنال

عنوان ژورنال: Ultrasound in Obstetrics and Gynecology

سال: 2007

ISSN: 0960-7692

DOI: 10.1002/uog.4971