Prenatal Diagnosis · 2000 · 14 citations · 22 references
MedicineObstetricsHuman GeneticsObstetric UltrasoundPrenatal DiagnosisCongenital Cranial AnomaliesFetal AnomaliesFetal Anomaly DetectionFetal ImagingFetal PathologyCongenital Anomaly Detection By UltrasonographyCorpus Callosum AbnormalitiesFetal Head UltrasonographyMolecular Prenatal ConfirmationMultifactorial EtiologyPrenatal Diagnosis Of MalformationsPrenatal Molecular DiagnosisSonographic Diagnostic Criteria
The recent identification of a common etiology among MASA syndrome (McKusick 303300), X-linked hydrocephalus (HSAS) (McKusick 307000) and other related neurological disorders, which had previously been considered distinct nosological entities, allowed us to diagnose MASA syndrome in a male fetus in a primigravida at the 29th week of gestation by sonographic signs of the MASA spectrum such as hydrocephalus and hypoplasia of corpus callosum. Indeed, the evidence of an X-linked neurological disease in the brother and the maternal uncle of the pregnant women enabled us to estimate a 25% risk of a male fetus being an affected hemizygote. The way in which a prenatal diagnosis, based on instrumental procedures, was reached is described since the authors were unable to perform, at the time of the observation, a molecular confirmation which was carried out only after birth.
22
MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM
Lieve Vits, Guy Van Camp, Paul Coucke et al. · Nature Genetics · 1994 · 154 citations
Genotype-phenotype correlation in L1 associated diseases.
Eric Fransen, Guy Van Camp, Rudi D’Hooge et al. · Journal of Medical Genetics · 1998 · 113 citations · Full text
The Syndrome of Sex-linked Hydrocephalus
James Edwards · Archives of Disease in Childhood · 1961 · 113 citations · Full text