Overview
Can Ficicioglu is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Philadelphia, Pennsylvania.
Dr. Ficicioglu is highly rated in 51 conditions, according to our data. His clinical expertise encompasses Classic Galactosemia, Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), Urea Cycle Disorders (UCD), and Gaucher Disease.
He is actively involved in clinical research, co-authoring 96 peer reviewed articles and participating in 14 clinical trials.
Specialties
Licenses
Hospital Affiliations
Languages Spoken
Gender
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- OTHER MEDICARE PART D
- PPO
- EPO
- HMO
- PPO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE SNP
- OTHER MEDICARE PART D
- HMO
- POS
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE SNP
- EPO
- HMO
- PPO
- EPO
- POS
- EPO
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE PART D
- EPO
- HMO
- POS
- PPO
- EPO
- PPO
- MEDICARE DISCOUNT CARD
- MEDICARE PDP
- OTHER MEDICARE
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
Locations
3401 Civic Ctr Blvd, Philadelphia, PA 19104
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.
14 Clinical Trials
Childrens Health Care Associates Inc
Elaine Zackai is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Philadelphia, Pennsylvania. Dr. Zackai is highly rated in 100 conditions, according to our data. Her clinical expertise encompasses Micrognathia, DiGeorge Syndrome, Hardikar Syndrome, Myringotomy, and Gastrostomy.
Jennifer Kalish is a Medical Genetics provider practicing medicine in Philadelphia, Pennsylvania. Dr. Kalish is highly rated in 19 conditions, according to our data. Her clinical expertise encompasses Beckwith-Wiedemann Syndrome, Macroglossia, Hemi 3 Syndrome, Glossectomy, and Pancreatectomy.
Nemours Children's Hospital, Delaware
Dr. Michael B. Bober is a pediatric geneticist and an authority on skeletal dysplasias, brittle bone disease, primordial dwarfism and other genetic disorders of the skeleton. He is a frequent guest lecturer, accomplished author and consultant for numerous television networks, here and abroad. Dr. Bober is highly rated in 69 conditions, according to our data. His clinical expertise encompasses Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD2), Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1), Achondroplasia, Osteotomy, and Adenoidectomy. Dr. Bober is board certified in American Board Of Medical Genetics And Genomics.
Frequently Asked Questions about Dr. Can H. Ficicioglu
How do I make an appointment with Dr. Can H. Ficicioglu?
You can book an appointment with Dr. Can H. Ficicioglu by calling their office at 215-590-1000. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Can H. Ficicioglu a top-rated expert for Classic Galactosemia?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Can H. Ficicioglu is classified as an Distinguished expert for Classic Galactosemia, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
What conditions does Dr. Can H. Ficicioglu specialize in?
While Dr. Can H. Ficicioglu is a Medical Genetics, they have specific expertise in Classic Galactosemia, Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), and Urea Cycle Disorders (UCD). MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Can H. Ficicioglu participate in research or clinical trials?
Yes. Dr. Can H. Ficicioglu has published 96 articles and abstracts on conditions like Classic Galactosemia. You can view a list of Dr. Can H. Ficicioglu's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Can H. Ficicioglu accept my insurance?
Dr. Can H. Ficicioglu accepts most major insurance plans, including Aetna and Anthem BCBS. We recommend calling the office directly at 215-590-1000 to verify that your specific plan is currently accepted before your visit.
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
- Argininosuccinic AciduriaDr. Ficicioglu isDistinguished. Learn about Argininosuccinic Aciduria.
- Cholesteryl Ester Storage DiseaseDr. Ficicioglu isDistinguished. Learn about Cholesteryl Ester Storage Disease.
- CitrullinemiaDr. Ficicioglu isDistinguished. Learn about Citrullinemia.
- Classic GalactosemiaDr. Ficicioglu isDistinguished. Learn about Classic Galactosemia.
- Galactokinase DeficiencyDr. Ficicioglu isDistinguished. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyDr. Ficicioglu isDistinguished. Learn about Galactose Epimerase Deficiency.
- Advanced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Arginase DeficiencyDr. Ficicioglu isAdvanced. Learn about Arginase Deficiency.
- Beta-Ketothiolase DeficiencyDr. Ficicioglu isAdvanced. Learn about Beta-Ketothiolase Deficiency.
- Biotinidase DeficiencyDr. Ficicioglu isAdvanced. Learn about Biotinidase Deficiency.
- Cardiomyopathy Hypogonadism Metabolic Anomalies
- Chondrodysplasia Punctata with Steroid Sulfatase Deficiency
- Experienced
- Achalasia Microcephaly SyndromeDr. Ficicioglu isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Activated PI3K Delta Syndrome (APDS)Dr. Ficicioglu isExperienced. Learn about Activated PI3K Delta Syndrome (APDS).
- Adrenal Insufficiency PediatricDr. Ficicioglu isExperienced. Learn about Adrenal Insufficiency Pediatric.
- Adrenoleukodystrophy (ALD)Dr. Ficicioglu isExperienced. Learn about Adrenoleukodystrophy (ALD).
- Alpha MannosidosisDr. Ficicioglu isExperienced. Learn about Alpha Mannosidosis.
- AminoaciduriaDr. Ficicioglu isExperienced. Learn about Aminoaciduria.