Richard J. Schroer
Experienced in Dihydropteridine Reductase Deficiency

Dr. Richard J. Schroer

Medical Genetics
Prisma Health
Greenwood Genetic Center– Charleston
3520 West Montague Avenue, 
Charleston, SC 
On Staff At
Accepting New Patients

Experienced in Dihydropteridine Reductase Deficiency
Prisma Health
Greenwood Genetic Center– Charleston
3520 West Montague Avenue, 
Charleston, SC 
OverviewInsuranceLocationsClinical ResearchSimilar Doctors

Overview

Richard Schroer is a Medical Genetics provider in Charleston, South Carolina. Dr. Schroer is rated as an Experienced provider by MediFind in the treatment of Dihydropteridine Reductase Deficiency. His top areas of expertise are Chromosome 2p Duplication, Propionic Acidemia, Phenylketonuria (PKU), and 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. Dr. Schroer is currently accepting new patients.

His clinical research consists of co-authoring 8 peer reviewed articles. MediFind looks at clinical research from the past 15 years.

Specialties
Medical Genetics
Licenses
Clinical Genetics in SC
Languages Spoken
English
Gender
Male

Insurance

Accepted insurance can change. Please verify directly with the provider.

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Accepted insurance plans:

Blue Cross Blue Shield
  • EPO
  • HMO
  • POS
  • PPO
Cigna
  • EPO
  • HMO
  • PPO
Humana
  • HMO
  • INDEMNITY
  • POS
  • PPO
Independent Health
  • EPO
  • POS
  • PPO
Medicaid
  • OTHER MEDICAID
  • STATE MEDICAID
UnitedHealthcare
  • EPO
  • HMO
  • POS
  • PPO
Wellcare
  • EPO
  • HMO
  • INSURANCE PLAN
  • MANAGED MEDICAID PLAN
  • MEDICARE MAPD
  • MEDICARE PDP
  • MEDICARE SNP
  • MEDICARE-MEDICAID PLAN
  • OTHER MEDICARE
  • OTHER MEDICARE PART D
View 2 Less Insurance Carriers -

Locations

Greenwood Genetic Center– Charleston
3520 West Montague Avenue, Charleston, SC 29418
Call: 843-746-1001

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.


8 Total Publications

Missense variants in CMS22 patients reveal that PREPL has both enzymatic and nonenzymatic functions.
Missense variants in CMS22 patients reveal that PREPL has both enzymatic and nonenzymatic functions.
Journal: JCI insight
Published: January 11, 2024
View All 8 Publications
Similar Doctors
Experienced in Dihydropteridine Reductase Deficiency
Dr. Neena Champaigne
Medical Genetics | Pediatrics
Experienced in Dihydropteridine Reductase Deficiency
Dr. Neena Champaigne
Medical Genetics | Pediatrics

University Medical Associates Of The Medical University Of South Carol

171 Ashley Ave, 
Charleston, SC 
 (7.0 miles away)
843-792-1414
Languages Spoken:
English
See accepted insurances
Offers Telehealth

Neena Champaigne is a Medical Genetics specialist and a Pediatrics provider in Charleston, South Carolina. Dr. Champaigne is rated as an Advanced provider by MediFind in the treatment of Dihydropteridine Reductase Deficiency. Her top areas of expertise are Rhizomelic Syndrome, Ornithine Translocase Deficiency, Ornithine Transcarbamylase Deficiency, and Classic Galactosemia.

VIEW MORE DIHYDROPTERIDINE REDUCTASE DEFICIENCY DOCTORS

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

Find Dr. Schroer's expertise for a condition
ConditionClose
      • Advanced
      • Chromosome 2p Duplication
        Dr. Schroer is
        Advanced
        . Learn about Chromosome 2p Duplication.
        See more Chromosome 2p Duplication experts
      • Experienced
      • 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
        Dr. Schroer is
        Experienced
        . Learn about 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency.
        See more 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency experts
      • Argininosuccinic Aciduria
        Dr. Schroer is
        Experienced
        . Learn about Argininosuccinic Aciduria.
        See more Argininosuccinic Aciduria experts
      • Autism Spectrum Disorder
        Dr. Schroer is
        Experienced
        . Learn about Autism Spectrum Disorder.
        See more Autism Spectrum Disorder experts
      • Dihydropteridine Reductase Deficiency
        Dr. Schroer is
        Experienced
        . Learn about Dihydropteridine Reductase Deficiency.
        See more Dihydropteridine Reductase Deficiency experts
      • Glutaric Acidemia Type 2
        Dr. Schroer is
        Experienced
        . Learn about Glutaric Acidemia Type 2.
        See more Glutaric Acidemia Type 2 experts
      • Increased Head Circumference
        Dr. Schroer is
        Experienced
        . Learn about Increased Head Circumference.
        See more Increased Head Circumference experts
      View All 9 Experienced Conditions
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