Gerald V. Raymond
Advanced in Metachromatic Leukodystrophy

Dr. Gerald V. Raymond

Pediatrics | Medical Genetics
Johns Hopkins Medicine
Rubenstein Child Health Building
Baltimore, MD 

Advanced in Metachromatic Leukodystrophy
Johns Hopkins Medicine
Rubenstein Child Health Building
Baltimore, MD 
OverviewInsuranceLocationsClinical ResearchSimilar Doctors

Overview

Dr. Gerald Raymond is a clinical geneticist and neurologist at Johns Hopkins where he is also a professor of genetic medicine and neurology. He obtained his MD at the University of Connecticut and was trained in Pediatrics at Johns Hopkins Hospital and Neurology at the Mass. General Hospital. He received additional training in developmental neuropathology at the Universite Catholique de Louvain in Belgium and clinical genetics at the Harvard Program. Dr. Raymond’s research has been at the overlap of genetics and neurology with specific focus on peroxisomal disorders including adrenoleukodystrophy. He has been actively involved in newborn screening for ALD and in developing clinical follow-up programs. He has extensive experience in clinical management of neurogenetic issues including peroxisomal and lysosomal disorders. He presently serves as the Director of the Lysosomal Storage Disease program in the department of Genetic Medicine.

Dr. Raymond is rated as an Advanced provider by MediFind in the treatment of Metachromatic Leukodystrophy. His top areas of expertise are Adrenoleukodystrophy (ALD), Leukodystrophy, Pelizaeus-Merzbacher Disease, and Alexander Disease.

Residency
Massachusetts General Hospital, Neurology, 1989
Specialties
Pediatrics
Medical Genetics
Licenses
Pediatrics in PA
Board Certifications
American Board Of Medical Genetics And Genomics
American Board Of Psychiatry And Neurology
Fellowships
Massachusetts General Hospital, Genetics, 1993
Universite Catholique De Louvaine Ucl 5020, Neuropathology, 1990
Hospital Affiliations
The Johns Hopkins Hospital
Languages Spoken
English
Gender
Male

Insurance

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

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Accepted insurance plans:

Aetna
  • EPO
  • HMO
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Anthem BCBS
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First Health
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Health Care Services Corporation
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  • OTHER MEDICARE
  • OTHER MEDICARE PART D
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HealthPartners
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Humana
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Johns Hopkins Healthcare
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Walgreens
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Wellcare
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  • MEDICARE SNP
  • MEDICARE-MEDICAID PLAN
  • OTHER MEDICARE
  • OTHER MEDICARE PART D
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Locations

Rubenstein Child Health Building
Rubenstein BLDG Lower Level, Baltimore, MD 21287
Call: 443-287-9494

Additional Areas of Focus

Dr. Raymond has provided the following conditions as areas of focus. Please note that we may not have enough data to validate their experience in some of these conditions.

Neurofibromatosis Type 1 (NF1)

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.


60 Total Publications

Maternal cobalamin deficiency causing infantile seizures and developmental regression.
Maternal cobalamin deficiency causing infantile seizures and developmental regression.
Journal: BMJ case reports
Published: November 12, 2025
View All 60 Publications
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Amena Fine is a Pediatrics provider in Baltimore, Maryland. Dr. Fine is rated as an Advanced provider by MediFind in the treatment of Metachromatic Leukodystrophy. Her top areas of expertise are Adrenoleukodystrophy (ALD), CACH Syndrome, HNRNPH2-Related Disorder, and Alexander Disease.

Sara E. Mixter
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Experienced in Metachromatic Leukodystrophy
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Johns Hopkins Outpatient Center

601 North Caroline Street, Floor 7, Floor 7, 
Baltimore, MD 
 (1.1 miles away)
410-955-0670
Languages Spoken:
English
See accepted insurances
Offers Telehealth

Dr. Sara Mixter is Assistant Professor of Medicine and Pediatrics at the Johns Hopkins University School of Medicine. Her areas of clinical expertise are internal medicine, pediatrics, and primary care for adults with developmental disabilities and other complex childhood-onset conditions. She is the director of the Hopkins PACT (Pediatric-informed Adult Care and Transition) Clinic. Dr. Mixter is also the medical director of the Pediatric Complex Care Collaborative (PC3) for the Johns Hopkins Children’s Center. Dr. Mixter received her A.B. from Harvard College. She earned her M.D. from Harvard Medical School and M.P.H. from the Harvard School of Public Health. She completed her residency at Johns Hopkins as part of the inaugural group of trainees in the Urban Health Combined Internal Medicine-Pediatrics Residency Program. Her research interests include transitions of care for adolescents with special healthcare needs and education for residents and medical students, especially in primary care and complex care. Dr. Mixter has served as the Assistant Chief of Service for the Longcope firm of the Osler Medical Housestaff Training Program (2015-16), as well as Assistant Program Director for Ambulatory Education (2014-15). Dr. Mixter is rated as an Advanced provider by MediFind in the treatment of Metachromatic Leukodystrophy. Her top areas of expertise are Cerebral Palsy, Gastroparesis, Orbital Cellulitis, and Sickle Cell Disease.

Experienced in Metachromatic Leukodystrophy
Dr. Chitra Vaidy
Pediatrics | General Practice
Experienced in Metachromatic Leukodystrophy
Dr. Chitra Vaidy
Pediatrics | General Practice
200 Cleaver Farm Rd Ste 201, Nemours Dupont Pediatrics, Middletown, 
Middletown, DE 
 (50.9 miles away)
302-378-5100
Languages Spoken:
English, Tamil, Telugu
See accepted insurances
Accepting New Patients

Chitra Vaidy is a primary care provider, a Pediatrics specialist and a General Practice provider in Middletown, Delaware. Dr. Vaidy is rated as an Advanced provider by MediFind in the treatment of Metachromatic Leukodystrophy. Her top areas of expertise are Food Allergy, Obesity in Children, Common Cold, and Pityriasis Rosea. Dr. Vaidy is currently accepting new patients.

VIEW MORE METACHROMATIC LEUKODYSTROPHY 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. Raymond's expertise for a condition
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      • Advanced
      • Adrenoleukodystrophy (ALD)
        Dr. Raymond is
        Advanced
        . Learn about Adrenoleukodystrophy (ALD).
        See more Adrenoleukodystrophy (ALD) experts
      • Alexander Disease
        Dr. Raymond is
        Advanced
        . Learn about Alexander Disease.
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      • CACH Syndrome
        Dr. Raymond is
        Advanced
        . Learn about CACH Syndrome.
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      • Canavan Disease
        Dr. Raymond is
        Advanced
        . Learn about Canavan Disease.
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      • Danon Disease
        Dr. Raymond is
        Advanced
        . Learn about Danon Disease.
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      • Farber Lipogranulomatosis
        Dr. Raymond is
        Advanced
        . Learn about Farber Lipogranulomatosis.
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      View All 21 Advanced Conditions
      • Experienced
      • 2q37 Deletion Syndrome
        Dr. Raymond is
        Experienced
        . Learn about 2q37 Deletion Syndrome.
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      • 47 XYY Syndrome
        Dr. Raymond is
        Experienced
        . Learn about 47 XYY Syndrome.
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      • Aase Syndrome
        Dr. Raymond is
        Experienced
        . Learn about Aase Syndrome.
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      • Abruzzo-Erickson Syndrome
        Dr. Raymond is
        Experienced
        . Learn about Abruzzo-Erickson Syndrome.
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      • Acrodermatitis Enteropathica
        Dr. Raymond is
        Experienced
        . Learn about Acrodermatitis Enteropathica.
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      • Acrorenal Mandibular Syndrome
        Dr. Raymond is
        Experienced
        . Learn about Acrorenal Mandibular Syndrome.
        See more Acrorenal Mandibular Syndrome experts
      View All 98 Experienced Conditions
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