Dr. Mary Norton is a Maternal Fetal Medicine specialist as well as a clinical geneticist. She specializes in the care of women at high risk for having a baby with a birth defect or genetic disorder. She oversees the prenatal diagnosis program at UCSF, and is an expert in high-risk obstetrical ultrasound and prenatal diagnosis procedures such as amniocentesis and CVS. Her research interests include the use of new genetic technologies for fetal testing, and she is a national expert in the use of cell free DNA testing. She also has a particular interest in patient attitudes and preferences regarding prenatal testing.
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Conditions: Hypertensive Disorders of Pregnancy,Preeclampsia,High Blood Pressure,Eclampsia,Pregnancy
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Conditions: Fetal Structural Anomalies
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Conditions: Hydrops Fetalis,Birth Defects
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Conditions: Sleep Apnea,Sleep Disorders,Preeclampsia,Obstetric Complication,CPAP,Eclampsia
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Conditions: Structural Anomalies,Cardiac Anomalies,Central Nervous System Anomalies,Thorax Anomalies,Genito-urinary Anomalies,Gastrointestinal Anomalies,Skeletal Anomalies,Multiple Anomalies,Congenital Heart Defects
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Conditions: Birth Defects,Intellectual Disability,Multiple Congenital Anomaly,Metabolic Disease,Epilepsy,Neurodegenerative Disease,Cerebral Palsy,Developmental Delay,Developmental Defect
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Conditions: Early Labor
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Conditions: Short Cervical Length
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Conditions: High Blood Pressure,Pregnancy
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Conditions: 22q11 Deletion Syndrome,DiGeorge Syndrome,Down Syndrome,Trisomy 13,Trisomy 18,Monosomy X,Sex Chromosome Abnormalities,Cri-du-Chat Syndrome,Angelman Syndrome,Prader-Willi Syndrome,1p36 Deletion Syndrome
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Sponsor: NIH K12HD001262
Role: Principal Investigator
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Sponsor: NIH U01HG009599
Role: Co-Principal Investigator
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Sponsor: NIH U10HD068268
Role: Co-Principal Investigator