| Literature DB >> 24839128 |
Claudia Cesaretti1, Luigina Spaccini, Mariangela Rustico, Cecilia Parazzini, Chiara Doneda, Thomas J Re, Andrea Righini.
Abstract
Hypochondroplasia (HCH) is a genetic skeletal dysplasia, inherited in an autosomal dominant fashion. About 50-70% of HCH patients have a mutation in FGFR3 gene and in the majority of cases it is a de novo mutation. Recent magnetic resonance imaging studies on relative large cohorts of HCH patients have showed a central nervous system involvement with a high incidence of characteristic temporal lobe and hippocampal abnormalities. To the best of our knowledge, this report shows the first magnetic resonance imaging prenatal detection of characteristic brain anomalies in a case of HCH, molecularly confirmed through postnatal FGFR3 analysis.Entities:
Mesh:
Year: 2014 PMID: 24839128 DOI: 10.1002/pd.4415
Source DB: PubMed Journal: Prenat Diagn ISSN: 0197-3851 Impact factor: 3.050