Overview
Natario Couser is an Ophthalmologist and a Medical Genetics provider in Baltimore, Maryland. Dr. Couser is rated as an Experienced provider by MediFind in the treatment of Homocystinuria. His top areas of expertise are Epicanthal Folds, Strabismus, Brown Syndrome, and Hypotonia.
His clinical research consists of co-authoring 52 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 1 article in the study of Homocystinuria.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- POS
- HMO
- INDEMNITY
- POS
- PPO
- HMO
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE-MEDICAID PLAN
- EPO
- HMO
- PPO
- HMO
- POS
Locations
200 N Wolfe St, Baltimore, MD 21287
Additional Areas of Focus
Dr. Couser 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.
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.
Charles Venditti is a Medical Genetics provider in Bethesda, Maryland. Dr. Venditti is rated as a Distinguished provider by MediFind in the treatment of Homocystinuria. His top areas of expertise are Methylmalonic Acidemia, Propionic Acidemia, Homocystinuria, and Niemann-Pick Disease.
Meral Gunay-Aygun is a Medical Genetics specialist and a Pediatrics provider in Bethesda, Maryland. Dr. Gunay-Aygun is rated as an Advanced provider by MediFind in the treatment of Homocystinuria. Her top areas of expertise are Phenylketonuria (PKU), Ornithine Translocase Deficiency, Ornithine Transcarbamylase Deficiency, and Argininosuccinic Aciduria. Dr. Gunay-Aygun is currently accepting new patients.
Hind Alsharhan is a Medical Genetics specialist and a Pediatrics provider in Baltimore, Maryland. Dr. Alsharhan is rated as an Experienced provider by MediFind in the treatment of Homocystinuria. Her top areas of expertise are ALG3-CDG, Ornithine Transcarbamylase Deficiency, Coenzyme Q Cytochrome C Reductase Deficiency, and Phenylketonuria (PKU). Dr. Alsharhan 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
- Distinguished
- Epicanthal FoldsDr. Couser isDistinguished. Learn about Epicanthal Folds.
- Advanced
- Brown SyndromeDr. Couser isAdvanced. Learn about Brown Syndrome.
- Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia
- Camptodactyly Syndrome Guadalajara Type 1
- Camptodactyly Syndrome Guadalajara Type 2
- Camptodactyly TaurinuriaDr. Couser isAdvanced. Learn about Camptodactyly Taurinuria.
- ColobomaDr. Couser isAdvanced. Learn about Coloboma.
- Experienced
- 15q11.2 MicrodeletionDr. Couser isExperienced. Learn about 15q11.2 Microdeletion.
- 2q37 Deletion SyndromeDr. Couser isExperienced. Learn about 2q37 Deletion Syndrome.
- 3p Deletion SyndromeDr. Couser isExperienced. Learn about 3p Deletion Syndrome.
- 47 XYY SyndromeDr. Couser isExperienced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Couser isExperienced. Learn about Aase Syndrome.
- Abruzzo-Erickson SyndromeDr. Couser isExperienced. Learn about Abruzzo-Erickson Syndrome.