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Verbeek S, Eilers PH, Lawrence K, Hennekam RC, Versteegh FG: Growth charts for children with Ellis-van Creveld syndrome.
Sequencing EVC and EVC2 identifies mutations in two-thirds of Ellis-van Creveld syndrome patients.
1,2) According to the literature, it has also been associated with some systemic conditions such as Mohr syndrome (Orofacial-digital talon cusp) (9), Sturge-weber syndrome (10), Rubinstein-Taybi syndrome (11), incontinentia pigmenti achromians and Ellis-Van creveld syndrome.
Bone dysplasia--Morquio's syndrome, Ellis-Van Creveld syndrome, Ollier's disease(multiple enchondromatosis), multiple hereditary exostosis, metaphyseal dysplasia, multiple epiphyseal dysplasia 8.
Congenitally missing teeth are seen in Witkop syndrome, Book syndrome, hypohidrotic ectodermal dysplasia, incontinentia pigmenti, Ellis-van Creveld syndrome, Hallermann-Streiff syndrome, focal dermal hypoplasia, lipoid proteinosis, Rieger syndrome, otodental dysplasia, Coffin-Lowry syndrome, trichodental syndrome and others.