Overview
Parith Wongkittichote is a Medical Genetics specialist and a Pediatrics provider in Philadelphia, Pennsylvania. Dr. Wongkittichote is highly rated in 6 conditions, according to our data. His top areas of expertise are Dihydrolipoamide Dehydrogenase Deficiency, Hypotonia, Glutaric Acidemia Type 1, and Multiple Sulfatase Deficiency.
His clinical research consists of co-authoring 37 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:
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE SNP
- EPO
- POS
- EPO
- 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.
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Jennifer Kalish is a Medical Genetics provider in Philadelphia, Pennsylvania. Dr. Kalish is highly rated in 19 conditions, according to our data. Her top areas of expertise are Beckwith-Wiedemann Syndrome, Macroglossia, Hemi 3 Syndrome, Hemihyperplasia, and Glossectomy.
Nemours Children's Hospital, Delaware
Dr. Michael B. Bober is a pediatric geneticist and an authority on skeletal dysplasias, brittle bone disease, primordial dwarfism and other genetic disorders of the skeleton. He is a frequent guest lecturer, accomplished author and consultant for numerous television networks, here and abroad. Dr. Bober is highly rated in 70 conditions, according to our data. His top areas of expertise are Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD2), Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1), Achondroplasia, Osteotomy, and Adenoidectomy.
Frequently Asked Questions about Dr. Parith Wongkittichote
How do I make an appointment with Dr. Parith Wongkittichote?
You can book an appointment with Dr. Parith Wongkittichote by calling their office at 267-426-7868. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Parith Wongkittichote a top-rated expert for Dihydrolipoamide Dehydrogenase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Parith Wongkittichote is classified as an Advanced expert for Dihydrolipoamide Dehydrogenase Deficiency, 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. Parith Wongkittichote specialize in?
While Dr. Parith Wongkittichote is a Medical Genetics, they have specific expertise in Dihydrolipoamide Dehydrogenase Deficiency, Hypotonia, and Glutaric Acidemia Type 1. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Parith Wongkittichote participate in research or clinical trials?
Yes. Dr. Parith Wongkittichote has published 37 articles and abstracts on conditions like Dihydrolipoamide Dehydrogenase Deficiency. You can view a list of Dr. Parith Wongkittichote's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Parith Wongkittichote accept my insurance?
Dr. Parith Wongkittichote accepts most major insurance plans, including Health Partners Plans and Horizon Healthcare. We recommend calling the office directly at 267-426-7868 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
- Advanced
- Dihydrolipoamide Dehydrogenase DeficiencyDr. Wongkittichote isAdvanced. Learn about Dihydrolipoamide Dehydrogenase Deficiency.
- Glutaric Acidemia Type 1Dr. Wongkittichote isAdvanced. Learn about Glutaric Acidemia Type 1.
- HypotoniaDr. Wongkittichote isAdvanced. Learn about Hypotonia.
- Maple Syrup Urine DiseaseDr. Wongkittichote isAdvanced. Learn about Maple Syrup Urine Disease.
- Mucolipidosis Type 4Dr. Wongkittichote isAdvanced. Learn about Mucolipidosis Type 4.
- Multiple Sulfatase DeficiencyDr. Wongkittichote isAdvanced. Learn about Multiple Sulfatase Deficiency.
- Experienced
- Atresia of Small IntestineDr. Wongkittichote isExperienced. Learn about Atresia of Small Intestine.
- CitrullinemiaDr. Wongkittichote isExperienced. Learn about Citrullinemia.
- Epilepsy in ChildrenDr. Wongkittichote isExperienced. Learn about Epilepsy in Children.
- MacrosomiaDr. Wongkittichote isExperienced. Learn about Macrosomia.
- Methylmalonic AcidemiaDr. Wongkittichote isExperienced. Learn about Methylmalonic Acidemia.
- Mucolipidosis 3Dr. Wongkittichote isExperienced. Learn about Mucolipidosis 3.