Indian Journal of Dermatology Venereology and Leprology · 2010 · 10 citations · 5 references
MedicineCraniofacial BiologyCraniofacial GeneticsCraniofacial GrowthHuman GeneticsCongenital Craniofacial AnomaliesCongenital Heart DiseaseCraniofacial AnomaliesDevelopmental Anomaly ImagingEctodermal DysplasiasSkeletal DysplasiasAssociated Craniofacial AnomaliesAutosomal Recessive InheritanceCongenital Craniofacial Anomalies GeneticsEctodermal Dysplasia SyndromesEllis-van Creveld Syndrome
Ellis-van Creveld (EVC) syndrome is a rare autosomal recessive congenital disorder characterized by chondrodysplasia and polydactyly, ectodermal dysplasia and congenital defects of the heart. We present here a case of a 16-year-old short-limbed dwarf with skeletal deformities and bilateral postaxial polydactyly, dysplastic nails and teeth, also having left-sided facial hemiatrophy. The diagnosis of EVC syndrome was made on the basis of clinical and radiological features. To the best of our knowledge, this is the first report of EVC syndrome with facial hemiatrophy in the medical literature from India.
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A new gene, EVC2, is mutated in Ellis–van Creveld syndrome
Marzena Galdzicka, Sujatha Patnala, M.G Hirshman et al. · Molecular Genetics and Metabolism · 2002 · 130 citations
Intracranial findings in progressive facial hemiatrophy.
Fry Ja, Alejandro Alvarellos, Fink Cw et al. · PubMed · 1992 · 67 citations