Overview
Michael Lyons is a Medical Genetics specialist and a Pediatrics provider in North Charleston, South Carolina. Dr. Lyons is rated as an Experienced provider by MediFind in the treatment of Neurofibromatosis Type 1 (NF1). His top areas of expertise are Increased Head Circumference, Delayed Growth, Cortical Dysplasia, and Microcephaly.
His clinical research consists of co-authoring 224 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 2 articles in the study of Neurofibromatosis Type 1 (NF1).
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
Locations
Additional Areas of Focus
Dr. Lyons 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.
University Medical Associates Of The Medical University Of South Carol
Kristen Lancaster is a Medical Genetics specialist and a Pediatrics provider in Charleston, South Carolina. Dr. Lancaster is rated as an Experienced provider by MediFind in the treatment of Neurofibromatosis Type 1 (NF1). Her top areas of expertise are Autosomal Cleft Palate, Chromosome 6q Deletion, Chromosome 15q Deletion, and Chromosome 12p Deletion.
Gurpur Pai is a Medical Genetics specialist and a Developmental and Behavioral Pediatrics provider in Charleston, South Carolina. Dr. Pai is rated as an Advanced provider by MediFind in the treatment of Neurofibromatosis Type 1 (NF1). His top areas of expertise are Classic Galactosemia, Galactosemia, Galactose Epimerase Deficiency, and Methylmalonic Acidemia.
University Medical Associates Of The Medical University Of South Carol
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 Neurofibromatosis Type 1 (NF1). Her top areas of expertise are Rhizomelic Syndrome, Ornithine Transcarbamylase Deficiency, Ornithine Translocase Deficiency, and Classic Galactosemia.
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
- Achalasia Microcephaly SyndromeDr. Lyons isAdvanced. Learn about Achalasia Microcephaly Syndrome.
- BlepharophimosisDr. Lyons isAdvanced. Learn about Blepharophimosis.
- Cortical DysplasiaDr. Lyons isAdvanced. Learn about Cortical Dysplasia.
- Delayed GrowthDr. Lyons isAdvanced. Learn about Delayed Growth.
- Increased Head CircumferenceDr. Lyons isAdvanced. Learn about Increased Head Circumference.
- MicrocephalyDr. Lyons isAdvanced. Learn about Microcephaly.
- Experienced
- 15q11.2 MicrodeletionDr. Lyons isExperienced. Learn about 15q11.2 Microdeletion.
- 2q37 Deletion SyndromeDr. Lyons isExperienced. Learn about 2q37 Deletion Syndrome.
- 47 XYY SyndromeDr. Lyons isExperienced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Lyons isExperienced. Learn about Aase Syndrome.
- Abruzzo-Erickson SyndromeDr. Lyons isExperienced. Learn about Abruzzo-Erickson Syndrome.
- Acrodermatitis EnteropathicaDr. Lyons isExperienced. Learn about Acrodermatitis Enteropathica.