| Literature DB >> 3560167 |
M M De Moor, R Baruch, D G Human.
Abstract
Three children with frontonasal dysplasia associated with tetralogy of Fallot are reported. All cases had true hypertelorism and a median nasal groove with absence of the nasal tip. There was no mental deficiency. The facial anomaly is a sporadic, non-genetic interference of the normal development of the face. This is the first report of frontonasal dysplasia associated with a cardiac defect. Multifactorial inheritance of this syndrome is proposed.Entities:
Mesh:
Year: 1987 PMID: 3560167 PMCID: PMC1049899 DOI: 10.1136/jmg.24.2.107
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318