Overview
Monica Penon-Portmann is a Pediatrics specialist and a Medical Genetics provider in San Francisco, California. Her top areas of expertise are Glycogen Storage Disease Type 0, Andersen Disease, Glycogen Storage Disease Type 9, and Glycogen Storage Disease Type 13. Dr. Penon-Portmann is currently accepting new patients.
Her clinical research consists of co-authoring 20 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Specialties
Licenses
Languages Spoken
Gender
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- INSURANCE PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER COMMERCIAL
- OTHER MEDICARE
- PPO
- EPO
- HMO
- PPO
- EPO
- HMO
- HMO
- MANAGED MEDICAID PLAN
- HMO
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- EPO
- PPO
- INSURANCE PLAN
- MEDICARE MAPD
- OTHER COMMERCIAL
- PPO
- EPO
- HMO
- POS
- PPO
Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
Lpch Medical Group Div Of Lucile
David Stevenson is a Medical Genetics specialist and a Pediatrics provider in Palo Alto, California. Dr. Stevenson is highly rated in 100 conditions, according to our data. His top areas of expertise are Neurofibromatosis Type 1 (NF1), Neurofibromatosis, RASopathies, Costello Syndrome, and Deep Brain Stimulation.
Ophir Klein is a Medical Genetics specialist and a Pediatrics provider in San Francisco, California. Dr. Klein is highly rated in 11 conditions, according to our data. His top areas of expertise are Costello Syndrome, RASopathies, Aplasia Cutis Congenita, and Clouston Syndrome.
Center For Complex Obstetric Medicine
Dr. Mary E. Norton is a perinatologist and clinical geneticist who cares for pregnant patients who have a fetus with a birth defect or genetic disorder or are at risk for such a condition. She performs obstetric ultrasounds, counsels patients with abnormal ultrasounds and performs prenatal tests like amniocentesis and chorionic villus sampling. She also interprets complex genetic tests, especially when abnormalities are found. Norton's areas of interest in research include applying new genetic tests to prenatal diagnosis and fetal disease, as well as patient decision-making around genetic testing and obstetrical ultrasound. She is co-director of the Center for Maternal-Fetal Precision Medicine at UCSF, as well as the David E. Thorburn, M.D. and Kate McKee Thorburn Endowed Chair in Perinatal Medicine and Genetics at UCSF. Norton earned her medical degree at the University of Washington. She completed a residency in obstetrics and gynecology at Tufts University followed by a fellowship in maternal-fetal medicine and clinical genetics at UCSF. After several years at Brigham and Women's Hospital and Harvard Medical School, she returned to San Francisco and joined UCSF Medical Center in 1998. Dr. Norton is highly rated in 23 conditions, according to our data. Her top areas of expertise are Fetal Edema, Hydrops Fetalis, Alpha Thalassemia, and Hemolytic Disease of the Newborn.
Frequently Asked Questions about Dr. Monica Penon-Portmann
How do I make an appointment with Dr. Monica Penon-Portmann?
You can book an appointment with Dr. Monica Penon-Portmann by calling their office at 415-476-2757. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Monica Penon-Portmann a top-rated expert for Glycogen Storage Disease Type 0?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Monica Penon-Portmann is classified as an Experienced expert for Glycogen Storage Disease Type 0, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
What conditions does Dr. Monica Penon-Portmann specialize in?
While Dr. Monica Penon-Portmann is a Pediatrics, they have specific expertise in Glycogen Storage Disease Type 0, Andersen Disease, and Glycogen Storage Disease Type 9. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Pediatrics.
Does Dr. Monica Penon-Portmann participate in research or clinical trials?
Yes. Dr. Monica Penon-Portmann has published 20 articles and abstracts on conditions like Glycogen Storage Disease Type 0. You can view a list of Dr. Monica Penon-Portmann's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Monica Penon-Portmann accept my insurance?
Dr. Monica Penon-Portmann accepts most major insurance plans, including Aetna and Cambia Health Solutions. We recommend calling the office directly at 415-476-2757 to verify that your specific plan is currently accepted before your visit.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Experienced
- Achalasia Microcephaly SyndromeDr. Penon-Portmann isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Acid Sphingomyelinase Deficiency (ASMD)Dr. Penon-Portmann isExperienced. Learn about Acid Sphingomyelinase Deficiency (ASMD).
- Adrenoleukodystrophy (ALD)Dr. Penon-Portmann isExperienced. Learn about Adrenoleukodystrophy (ALD).
- Alpha MannosidosisDr. Penon-Portmann isExperienced. Learn about Alpha Mannosidosis.
- Andersen DiseaseDr. Penon-Portmann isExperienced. Learn about Andersen Disease.
- Arthrogryposis Multiplex CongenitaDr. Penon-Portmann isExperienced. Learn about Arthrogryposis Multiplex Congenita.
