Overview
Catherine Keegan is a Medical Genetics specialist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Keegan is rated as an Experienced provider by MediFind in the treatment of Carbamoyl Phosphate Synthetase 1 Deficiency. Her top areas of expertise are Intersex, Aarskog Syndrome, Turner Syndrome, and Imperforate Anus.
Her clinical research consists of co-authoring 48 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:
- EPO
- HMO
- POS
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- HMO
- HMO
- POS
Locations
1500 E Medical Ctr Dr, 6th Floor Mott Hospital Rm, Ann Arbor, MI 48109
Additional Areas of Focus
Dr. Keegan 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.
Regents Of The University Of Michigan
Ayesha Ahmad is a Medical Genetics specialist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Ahmad is rated as a Distinguished provider by MediFind in the treatment of Carbamoyl Phosphate Synthetase 1 Deficiency. Her top areas of expertise are Pompe Disease, Propionic Acidemia, Von Gierke Disease, and Classic Galactosemia. Dr. Ahmad is currently accepting new patients.
Regents Of The University Of Michigan
Shane Quinonez is a Medical Genetics specialist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Quinonez is rated as a Distinguished provider by MediFind in the treatment of Carbamoyl Phosphate Synthetase 1 Deficiency. His top areas of expertise are Pompe Disease, Dihydrolipoamide Dehydrogenase Deficiency, MELAS Syndrome, and Propionic Acidemia.
Pioneer Medical Associates PC
Ghanem Sharabi is a primary care provider, practicing in Pediatrics and Internal Medicine in Warren, Michigan. Dr. Sharabi is rated as a Distinguished provider by MediFind in the treatment of Carbamoyl Phosphate Synthetase 1 Deficiency. His top areas of expertise are Glossitis, Pernicious Anemia, Necrosis, Gastrostomy, and Endoscopy. Dr. Sharabi 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
- IntersexDr. Keegan isDistinguished. Learn about Intersex.
- Advanced
- Aarskog SyndromeDr. Keegan isAdvanced. Learn about Aarskog Syndrome.
- Turner SyndromeDr. Keegan isAdvanced. Learn about Turner Syndrome.
- Experienced
- 5-Alpha Reductase DeficiencyDr. Keegan isExperienced. Learn about 5-Alpha Reductase Deficiency.
- Brachydactyly Mononen TypeDr. Keegan isExperienced. Learn about Brachydactyly Mononen Type.
- Carbamoyl Phosphate Synthetase 1 Deficiency
- Cortical DysplasiaDr. Keegan isExperienced. Learn about Cortical Dysplasia.
- Hydrocephalus due to Congenital Stenosis of Aqueduct of Sylvius
- HypospadiasDr. Keegan isExperienced. Learn about Hypospadias.