| Literature DB >> 7991518 |
A Salamanca1, F Gonzalez-Gomez, M C Padilla, M A Motos, F Zorrilla, R M Sabatel.
Abstract
Foramina parietalia permagna (FPP) is an extremely uncommon congenital defect, inherited as an autosomal dominant condition. Its characteristics are two symmetrical orifices in the parietal bones (not of fixed size) on both sides of the midline. This defect does not affect either the psychic or the physical development of the affected person. This paper describes the sonographic appearance of FPP in utero as an enlargement of the posterior fontanelle.Entities:
Mesh:
Year: 1994 PMID: 7991518 DOI: 10.1002/pd.1970140820
Source DB: PubMed Journal: Prenat Diagn ISSN: 0197-3851 Impact factor: 3.050