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Aortic Abnormalities: How to Identify Pediatric Patients at Risk
Pediatric cardiologist Emilio Quezada, MD, discusses signs that a young patient should be evaluated for genetic syndromes associated with thoracic aorta dilation and aneurysm.
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Congenital Heart Disease: The Value and Future of Fetal Screening
With CHD often discovered in low-risk pregnancies and associated with neurodevelopmental deficits, the need for more screening and advanced techniques is clear.
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The Potential of Fetal MRI: Delivering Value Now and in the Future
UCSF pediatric radiology specialists address fetal MRI safety concerns and explain when to consider advanced imaging.
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Hard Facts to Inform Hard Decisions: Treating the Fetal Heart
Anita J. Moon-Grady, MD, FAAP, director of the UCSF Fetal Cardiovascular Program, examines the reality of whether long-term outcomes are better for babies who had in utero interventions for certain heart defects, as well as the short-term complications for mothers.
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Genetic Diseases Linked to Nonimmune Hydrops: Distinctions in Diagnosis and Prognosis
In this short video, Maternal-Fetal Medicine and Genetics specialist, Dr. Teresa Sparks, MD, MAS, presents a recently published UCSF study of non-immune hydrops fetalis (NIHF) cases.
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Fetal Neurology: New Frontiers
Ventriculomegaly and corpus callosum abnormalities are relatively common fetal ultrasound findings involving the brain. Neuroimaging specialists at the UCSF Fetal Treatment Center illustrate their consult process, showing the prognostic range for these conditions and MRI’s potential payoff for patient management.
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Placenta Accreta Spectrum Disorder: Proven Strategies from a Multidisciplinary Team
Placenta accreta spectrum disorder is a varied and increasingly common complication of pregnancy, so ob/gyns need a firm grasp of risk factors and ultrasound signs
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Tippi, Elliott and Elianna’s Story: Little Girl Thrives After Fetal Stem Cell Transplant: Part 2
Working with a team of more than 100 UCSF specialists, Tippi MacKenzie, MD, and Elliott Vichinsky, MD, are leading work to bring cutting edge therapies to patients with genetic blood disorders.
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Tippi and Elianna’s Story: Stopping a Fatal Blood Disease Before Birth: Part 1
Tippi MacKenzie, MD, is stopping disease before it starts in the womb. In 2017, she launched the world's first clinical trial of an in-utero stem cell transplant therapy. Her first patient, baby Elianna, was born just four months later.
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Congenital Diaphragmatic Hernia: A Little Hole With Big Consequences
Specialists with the UCSF Fetal Treatment Center share the latest on prenatal techniques for detecting, evaluating and treating diaphragmatic hernias to optimize lung development and prevent deadly pulmonary hypertension. They also present intensive care strategies for newborns and long-term developmental care plans for kids.
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Exome Sequencing
Perinatologist and medical geneticist Mary Norton, discusses a genetic test called exome sequencing. With recent discoveries I'm genetics we can now test for many more genetic conditions.
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Genetic Testing Update: When Is Exome Sequencing Valuable in Prenatal Diagnosis?
In this webinar, maternal-fetal medicine and genetics specialists, Drs. Mary Norton and Teresa Sparks discuss advances in genetic testing.
