Dr. Kandamurugu Manickam
Overview
Kandamurugu Manickam is a Medical Genetics specialist and a Pediatrics provider in Toledo, Ohio. Dr. Manickam is rated as an Experienced provider by MediFind in the treatment of Hypotonia. His top areas of expertise are Chromosome 6q Deletion, Vici Syndrome, Neurofibromatosis Type 1 (NF1), and Miller-Dieker Syndrome. Dr. Manickam is currently accepting new patients.
His clinical research consists of co-authoring 48 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 Hypotonia.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- HMO
- HMO
- INDEMNITY
- POS
- PPO
- HMO
- EPO
- HMO
- PPO
- EPO
- HMO
- POS
- PPO
Locations
2222 Cherry Street, Suite 2600, Toledo, OH 43608
700 Childrens Drive, Columbus, OH 43205
Additional Areas of Focus
Dr. Manickam 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.
Kristin Monaghan is a Medical Genetics provider in Detroit, Michigan. Dr. Monaghan is rated as a Distinguished provider by MediFind in the treatment of Hypotonia. Her top areas of expertise are Hypotonia, 1p36 Deletion Syndrome, Microcephaly Deafness Syndrome, and Early Infantile Epileptic Encephalopathy.
Nationwide Children's Hospital Toledo-Genetics
Scott Hickey is a Medical Genetics specialist and a Pediatrics provider in Toledo, Ohio. Dr. Hickey is rated as a Distinguished provider by MediFind in the treatment of Hypotonia. His top areas of expertise are Cerebellar Hypoplasia, Micrognathia, Trisomy 3 Mosaicism, and Mosaicism. Dr. Hickey is currently accepting new patients.
Mark Hannibal is a Pediatrics specialist and a Medical Genetics provider in Ann Arbor, Michigan. Dr. Hannibal is rated as a Distinguished provider by MediFind in the treatment of Hypotonia. His top areas of expertise are Aase Syndrome, CHARGE Syndrome, Bowen-Conradi Syndrome, and Filippi 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
- Chromosome 6q DeletionDr. Manickam isElite. Learn about Chromosome 6q Deletion.
- Advanced
- Neurofibromatosis Type 1 (NF1)Dr. Manickam isAdvanced. Learn about Neurofibromatosis Type 1 (NF1).
- Vici SyndromeDr. Manickam isAdvanced. Learn about Vici Syndrome.
- Experienced
- 2q37 Deletion SyndromeDr. Manickam isExperienced. Learn about 2q37 Deletion Syndrome.
- 47 XYY SyndromeDr. Manickam isExperienced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Manickam isExperienced. Learn about Aase Syndrome.
- Abruzzo-Erickson SyndromeDr. Manickam isExperienced. Learn about Abruzzo-Erickson Syndrome.
- Achalasia Microcephaly SyndromeDr. Manickam isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Acrodermatitis EnteropathicaDr. Manickam isExperienced. Learn about Acrodermatitis Enteropathica.