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Cleidocranial dysostosis in a family with twins
Acta geneticae medicae et gemellologiae
A family is reported in which 5 individuals out of 2 generations were found to suffer from dysostosis cleidocranialis. In that kindred twins occurred twice, one twin pair being DZ and suffering from the disease, the other pair MZ and healthy. The number of affected family members is in agreement with the autosomal dominance of the trait as indicated by numerous earlier observations. The characteristics found were: reduced growth, macrocephalus with late fontanel occlusion, protrusive frontaldoi:10.1017/s1120962300013160 fatcat:znzhj4ekqra3tlt3iar67vduzm