Overview
Moin Vera is a Medical Genetics specialist and a Pediatrics provider in Los Angeles, California. Dr. Vera is rated as an Experienced provider by MediFind in the treatment of Chondrodystrophy. His top areas of expertise are Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Mucopolysaccharidoses (MPS), Triple X Syndrome, and Chromosome 10q Deletion.
His clinical research consists of co-authoring 14 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:
- OTHER MEDICAID
- STATE MEDICAID
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.
The Regents Of The University Of California
Deborah Krakow is a Medical Genetics specialist and an Obstetrics and Gynecologist in Los Angeles, California. Dr. Krakow is rated as an Elite provider by MediFind in the treatment of Chondrodystrophy. Her top areas of expertise are Osteogenesis Imperfecta, Acromicric Dysplasia, Chondrodystrophy, and Spondyloepimetaphyseal Dysplasia Strudwick Type.
Leslie Raffel is a Medical Genetics specialist and a Pediatrics provider in West Hollywood, California. Dr. Raffel is rated as an Advanced provider by MediFind in the treatment of Chondrodystrophy. Her top areas of expertise are Chromosome 13q Deletion, Miller-Dieker Syndrome, Smith-Magenis Syndrome, and HNRNPH2-Related Disorder.
Matthew Deardorff is a Medical Genetics specialist and a Pediatrics provider in Los Angeles, California. Dr. Deardorff is rated as an Elite provider by MediFind in the treatment of Chondrodystrophy. His top areas of expertise are Cornelia De Lange Syndrome, Coffin-Siris Syndrome, Mosaicism, and Beckwith-Wiedemann Syndrome.
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
- Elite
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Distinguished
- Mucopolysaccharidoses (MPS)Dr. Vera isDistinguished. Learn about Mucopolysaccharidoses (MPS).
- Advanced
- Adrenoleukodystrophy (ALD)Dr. Vera isAdvanced. Learn about Adrenoleukodystrophy (ALD).
- Biotinidase DeficiencyDr. Vera isAdvanced. Learn about Biotinidase Deficiency.
- Chromosome 10q DeletionDr. Vera isAdvanced. Learn about Chromosome 10q Deletion.
- Classic GalactosemiaDr. Vera isAdvanced. Learn about Classic Galactosemia.
- Dihydropteridine Reductase Deficiency
- Kearns-Sayre SyndromeDr. Vera isAdvanced. Learn about Kearns-Sayre Syndrome.
- Experienced
- 2q37 Deletion SyndromeDr. Vera isExperienced. Learn about 2q37 Deletion Syndrome.
- 3MC SyndromeDr. Vera isExperienced. Learn about 3MC Syndrome.
- 47 XYY SyndromeDr. Vera isExperienced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Vera isExperienced. Learn about Aase Syndrome.
- Abruzzo-Erickson SyndromeDr. Vera isExperienced. Learn about Abruzzo-Erickson Syndrome.
- AchondroplasiaDr. Vera isExperienced. Learn about Achondroplasia.