Overview
Howard Saal is a Medical Genetics specialist and a Pediatrics provider in Cincinnati, Ohio. Dr. Saal is highly rated in 18 conditions, according to our data. His top areas of expertise are Achondroplasia, Crouzon Syndrome, Acrofrontofacionasal Dysostosis Syndrome, and Treacher Collins Syndrome.
His clinical research consists of co-authoring 50 peer reviewed articles and participating in 3 clinical trials. MediFind looks at clinical research from the past 15 years.
Insurance
Please contact the provider to confirm they accept your insurance or if you don't see your insurance listed.
Accepted insurance plans
- Blue Cross Blue Shield
- Anthem
- Cambia Health Solutions
- CareSource
- Cigna
- Managed Medicaid
Locations
3333 Burnet Ave, Cincinnati, OH 45229
Additional Areas of Focus
Dr. Saal 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.
3 Clinical Trials
Children's Hospital Medical Center
Kathryn Weaver is a Medical Genetics specialist and a Pediatrics provider in Cincinnati, Ohio. Dr. Weaver has been practicing medicine for over 16 years is highly rated in 16 conditions, according to our data. Their top areas of expertise are Acrofacial Dysostosis Catania Type, RASopathies, Micrognathia, and Pierre Robin Sequence.
Children's Hospital Medical Center
Robert Hopkin is a Medical Genetics specialist and a Pediatrics provider in Cincinnati, Ohio. Dr. Hopkin is highly rated in 111 conditions, according to our data. His top areas of expertise are Fabry Disease, Micrognathia, Ohdo Syndrome, Say-Barber-Biesecker-Young-Simpson Variant, Multiple Sulfatase Deficiency, and Orchiectomy.
Children's Hospital Medical Center
Elizabeth Schorry is a Medical Genetics specialist and a Pediatrics provider in Cincinnati, Ohio. Dr. Schorry is highly rated in 11 conditions, according to our data. Her top areas of expertise are Neurofibromatosis Type 1 (NF1), Neurofibromatosis, Brittle Cornea Syndrome, and Vascular Ehlers-Danlos Syndrome (VEDS).
Areas of Expertise
When evaluating expertise, MediFind pulls from factors such as the 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.
To learn more about how MediFind determines the expertise levels, check out our expert tiers page.
- Elite
- Achondroplasia
- Distinguished
- Acrofacial Dysostosis Catania Type
- Acrofacial Dysostosis Rodriguez Type
- Acrofrontofacionasal Dysostosis Syndrome
- Crouzon Syndrome
- Micrognathia
- Pierre Robin Sequence
- Advanced
- Brachydactyly Mononen Type
- Chondrodystrophy
- Coloboma
- Craniosynostosis
- Hydranencephaly
- Hypophosphatasia (HPP)
- Experienced
- 3MC Syndrome
- Acromicric Dysplasia
- CHARGE Syndrome
- Choanal Atresia
- Coffin-Lowry Syndrome
- Coffin-Siris Syndrome