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Foramina parietalia permagna: report of nine cases in one family
1Department of Paediatrics, First Medical Faculty, Charles University, Prague, Czech Republic.
Journal of Paediatrics and Child Health
|April 1, 1997
Abstract:
Nine members of a family with foramina parietalia permagna (FPP), inherited as an autosomal dominant trait are reported. Although usually benign, FPP may be associated with other malformations.