Overview
Patricia Dickson is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Saint Louis, Missouri.
Dr. Dickson is highly rated in 12 conditions, according to our data. Her clinical expertise encompasses Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome), and Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B).
She is actively involved in clinical research, co-authoring 109 peer reviewed articles and participating in 1 clinical trial. Dr. Dickson is currently accepting new patients.
Specialties
Licenses
Hospital Affiliations
Languages Spoken
Gender
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE-MEDICAID PLAN
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- EPO
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
Locations
1 Childrens Pl, Saint Louis, MO 63110
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.
1 Clinical Trials
Washington University
Dorothy Grange is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Saint Louis, Missouri. Dr. Grange is highly rated in 20 conditions, according to our data. Her clinical expertise encompasses Phenylketonuria (PKU), Clouston Syndrome, Aplasia Cutis Congenita, and Ectodermal Dysplasias. Dr. Grange is currently accepting new patients.
Washington University
Gary Gottesman is a Medical Genetics specialist and an Endocrinologist practicing medicine in Saint Louis, Missouri. Dr. Gottesman is highly rated in 12 conditions, according to our data. His clinical expertise encompasses X-Linked Hypophosphatemia, Hypophosphatemia, Juvenile Paget's Disease, Rickets, and Leg or Foot Amputation. Dr. Gottesman is currently accepting new patients.
Washington University
Marwan Shinawi is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Town And Country, Missouri. Dr. Shinawi is highly rated in 25 conditions, according to our data. His clinical expertise encompasses Hypotonia, Polysyndactyly Cardiac Malformation, Osteopathia Striata Cranial Sclerosis, and Increased Head Circumference. Dr. Shinawi is currently accepting new patients.
Frequently Asked Questions about Dr. Patricia I. Dickson
How do I make an appointment with Dr. Patricia I. Dickson?
You can book an appointment with Dr. Patricia I. Dickson by calling their office at 314-454-6000. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Patricia I. Dickson a top-rated expert for Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Patricia I. Dickson is classified as an Elite expert for Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), 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. Patricia I. Dickson specialize in?
While Dr. Patricia I. Dickson is a Medical Genetics, they have specific expertise in Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Mucopolysaccharidoses (MPS), and Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome). MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Patricia I. Dickson participate in research or clinical trials?
Yes. Dr. Patricia I. Dickson has published 108 articles and abstracts on conditions like Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). You can view a list of Dr. Patricia I. Dickson's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Patricia I. Dickson accept my insurance?
Dr. Patricia I. Dickson accepts most major insurance plans, including Aetna and Anthem BCBS. We recommend calling the office directly at 314-454-6000 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
- Elite
- Mucopolysaccharidoses (MPS)Dr. Dickson isElite. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome)
- Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B)
- Distinguished
- Chromosome 9p DeletionDr. Dickson isDistinguished. Learn about Chromosome 9p Deletion.
- Advanced
- Batten DiseaseDr. Dickson isAdvanced. Learn about Batten Disease.
- CLN1 DiseaseDr. Dickson isAdvanced. Learn about CLN1 Disease.
- CLN2 DiseaseDr. Dickson isAdvanced. Learn about CLN2 Disease.
- CLN3 DiseaseDr. Dickson isAdvanced. Learn about CLN3 Disease.
- CLN4 DiseaseDr. Dickson isAdvanced. Learn about CLN4 Disease.
- CLN5 DiseaseDr. Dickson isAdvanced. Learn about CLN5 Disease.
- Niemann-Pick DiseaseDr. Dickson isAdvanced. Learn about Niemann-Pick Disease.
- Experienced
- AchondroplasiaDr. Dickson isExperienced. Learn about Achondroplasia.
- Acromicric DysplasiaDr. Dickson isExperienced. Learn about Acromicric Dysplasia.
- GangliosidosisDr. Dickson isExperienced. Learn about Gangliosidosis.
- Gastroesophageal Reflux in InfantsDr. Dickson isExperienced. Learn about Gastroesophageal Reflux in Infants.
- GM1 GangliosidosisDr. Dickson isExperienced. Learn about GM1 Gangliosidosis.
- HypotoniaDr. Dickson isExperienced. Learn about Hypotonia.
- Kabuki SyndromeDr. Dickson isExperienced. Learn about Kabuki Syndrome.
- Krabbe DiseaseDr. Dickson isExperienced. Learn about Krabbe Disease.
- Maple Syrup Urine DiseaseDr. Dickson isExperienced. Learn about Maple Syrup Urine Disease.
- Mucolipidosis 3Dr. Dickson isExperienced. Learn about Mucolipidosis 3.
- Mucolipidosis Type 4Dr. Dickson isExperienced. Learn about Mucolipidosis Type 4.
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Multiple Sulfatase DeficiencyDr. Dickson isExperienced. Learn about Multiple Sulfatase Deficiency.
- N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3
- Newborn Low Blood SugarDr. Dickson isExperienced. Learn about Newborn Low Blood Sugar.
- Pediatric MyocarditisDr. Dickson isExperienced. Learn about Pediatric Myocarditis.
- Polysyndactyly Cardiac MalformationDr. Dickson isExperienced. Learn about Polysyndactyly Cardiac Malformation.
- Retinopathy Pigmentary Mental RetardationDr. Dickson isExperienced. Learn about Retinopathy Pigmentary Mental Retardation.
- SialidosisDr. Dickson isExperienced. Learn about Sialidosis.
- SyndactylyDr. Dickson isExperienced. Learn about Syndactyly.
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency