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  • Title: [A family with the EEC syndrome (ectrodactily, ectodermal dysplasia clefting syndrome): clinical variability and genetic counseling].
    Author: Gualandri V, Ronzoni MG, Montagnani A, Orsini GB.
    Journal: J Fr Ophtalmol; 1986; 9(12):855-7. PubMed ID: 3571845.
    Abstract:
    In a family with segregation of EEC-Syndrome we observed five children--two girls and three males--(two of them dizygotic twins) affected by very various phenotypes of the syndrome. The ocular symptomatology was represented by agenesis or stenosis of lacrimal ducts: two children were operated, the other suffered from frequent inflammations. The study of the family suggest an autosomic dominant heredity with defect of penetrance on the father.
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