Overview
Shagun Kaur is a Pediatrics specialist and a Medical Genetics provider in Phoenix, Arizona. Dr. Kaur has been practicing medicine for over 9 years and is rated as an Experienced provider by MediFind in the treatment of HNRNPH2-Related Disorder. Her top areas of expertise are Classic Galactosemia, Galactose Epimerase Deficiency, Galactosemia, and Hydranencephaly. Dr. Kaur is currently accepting new patients.
Her clinical research consists of co-authoring 11 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
Accepted plan types not found. Please verify directly with the provider.
- HMO
- INDEMNITY
- POS
- PPO
- OTHER MANAGED MEDICAID
- EPO
- HMO
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- EPO
- HMO
- EPO
- HMO
- POS
- PPO
Locations
1919 E Thomas Rd, Phoenix, AZ 85016
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.
Theresa Grebe is a Medical Genetics specialist and a Pediatrics provider in Phoenix, Arizona. Dr. Grebe is rated as an Advanced provider by MediFind in the treatment of HNRNPH2-Related Disorder. Her top areas of expertise are Chromosome 6 Uniparental Disomy, Temple Syndrome, Hypotonia, and Chromosome 13q Duplication. Dr. Grebe is currently accepting new patients.
Phoenix Children's Hospital
Jasmine Knoll is a Medical Genetics specialist and a Pediatrics provider in Phoenix, Arizona. Dr. Knoll is rated as an Advanced provider by MediFind in the treatment of HNRNPH2-Related Disorder. Her top areas of expertise are Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), Fabry Disease, Multiple Sulfatase Deficiency, and Megalencephalic Leukoencephalopathy with Subcortical Cysts. Dr. Knoll is currently accepting new patients.
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
- Advanced
- Classic GalactosemiaDr. Kaur isAdvanced. Learn about Classic Galactosemia.
- Galactose Epimerase Deficiency
- GalactosemiaDr. Kaur isAdvanced. Learn about Galactosemia.
- HydranencephalyDr. Kaur isAdvanced. Learn about Hydranencephaly.
- Experienced
- 2q37 Deletion SyndromeDr. Kaur isExperienced. Learn about 2q37 Deletion Syndrome.
- 47 XYY SyndromeDr. Kaur isExperienced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Kaur isExperienced. Learn about Aase Syndrome.
- Abruzzo-Erickson SyndromeDr. Kaur isExperienced. Learn about Abruzzo-Erickson Syndrome.
- Achalasia Microcephaly SyndromeDr. Kaur isExperienced. Learn about Achalasia Microcephaly Syndrome.
- AcrocephalopolydactylyDr. Kaur isExperienced. Learn about Acrocephalopolydactyly.