Pediatrics Dr. Gamze Şarbat
✓ Medically verified profileDr. Gamze Şarbat
✓ Medically verified profile
About Dr. Gamze Şarbat
Quick answer
Dr. Gamze Şarbat is a Pediatrics specialist at Acibadem International in Turkey with 43+ years of experience.
She focuses on glycogen storage disease type I and type Ia, glucose-6-phosphatase deficiency, biotinidase deficiency, inherited and pediatric metabolic diseases, pediatric nutrition disorders, newborn screening for biotinidase deficiency, and well-child and preventive pediatric care. She consults in Turkish and English and offers online video consultation.
M.D. Gamze Şarbat is a pediatrician trained at Istanbul University Faculty of Medicine, graduating in 1994. She practiced general pediatrics at Maslak Acıbadem Hospital from 2010 to 2018, providing comprehensive care for infants, children, and adolescents. Dr. Şarbat is a member of the Istanbul Medical Chamber and remains dedicated to promoting child health through clinical excellence, preventive care, and family-centered practice.
Areas of Expertise
Conditions treated and procedures performed by this specialist.
Education
- 1994Istanbul University Istanbul Faculty of Medicine Pediatrics
- 1989Istanbul University Istanbul Faculty of Medicine
Professional Experience
- 2010–2018Maslak Acibadem Hospital General Pediatrics
- 2010Acibadem Health Group
- 2006–2009Etiler Acibadem Medical Center Healthy Child and General Pediatrics
- 2000–2006Kadikoy Acibadem Hospital General Pediatrics
- 1999–2000The University of Illinois at Chicago Department of Genetics and Metabolism Department of Pediatrics
- 1998–1999Pediatric Metabolic Diseases at the University of Illinois at Chicago
- 1994–2001Istanbul University Istanbul Faculty of Medicine, Department of Pediatrics, Division of Nutrition and Metabolism Chief Assistant
- 1989–1994Istanbul University Istanbul Faculty of Medicine Pediatrics Residency
- 1983–1989Istanbul University Istanbul Faculty of Medicine Medical Doctorate
Professional Memberships
- Istanbul Medical Chamber
Selected Publications
- The molecular basis of glycogen storage disease type Ia. J Biol Chem 277 (7): 5047-5053 (2002) Shieh JJ, Terzioglu M, Hiraiwa H, et al.
- Glycogen storage disease type I: diagnosis and phenotype/genotype correlation. Eur J Pediatr 161: S10-S19 Suppl. 1 OCT (2002) Matern D, Seydewitz HH, Bali D, et al.
- The catalytic center of glucose-6-phosphatase-HIS176 is the nucleophile forming the phosphohistidine-enzyme intermediate during catalysis. J Biol Chem 277 (36): 32837-32842 (2002) Ghosh A, Shieh JJ, Pan CJ, et al.
- Clinical and neuropsychological outcome in 33 patients with biotinidase deficiency ascertained by nationwide newborn screening and family studies in Austria. Eur J Pediatr 160 (5): 277-282 (2001) Moslinger D, Stockler-Ipsiroglu S, Scheibenreiter S, et al.
- Glucose-6-phosphatase gene mutation in Turkish patients with glycogen storage disease type Ia. Journal of Inherited Metabolic Disease 24 (8): 881-882 (2001) Terzioglu M, Emre S, Ozen H, et al.
- Molecular genetics of type I glycogen storage disease. Mol Genet Metab 73 (2): 117-125 (2001) Janecke AR, Mayatepek E, Utermann G.
- . Novel mutations cause biotinidase deficiency in Turkish children. Journal of Inherited Metabolic Disease 23 (2): 120-128 (2000) Pomponio RJ, Coskun T, Demirkol M, et al.
- Glycogen storage disease type Ia: recent experience with mutation analysis a summary of mutations reported in the literature and a newly developed diagnostic flowchart. Eur J Pediatr 159 (5): 322-330 (2000) Rake JP, ten Berge AM, Visser G, et al.
- Heterogeneous mutation in the glucose-6-phosphatase gene in Japanese patients with glycogen storage disease type Ia. Am J Med Genet 92 (2): 90-94 (2000) Takahashi K, Akanuma J, Matsubara Y, et al.
- Molecular aspects of glycogen storage disease type Ia in Turkish patients: a novel mutation in the glucose-6- phosphatase gene. J Inherit Metab Dis 21: 445-446 (1998) Hüner G, Podskarbi T, Schütz M, Baykal T, Şarbat G, Shin YS, Demirkol M.
- Incidence of biotinidase deficiency in Turkish newborns. T, Huner G, Sarbat G, et al. Acta Paediatrica 87 (10): 1102-1103 (1998)
- Five years experience in newborn screening for biotinidase deficiency in Istanbul. Enzyme Protein 49: 186-187 (1996) Demirkol M, Baykal T, Hüner G, Şarbat G, İnce Z, Cantez T.
Frequently Asked Questions
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A dedicated team, from first message to follow-up
Our international patient office coordinates your appointment, travel and treatment at JCI-accredited Acıbadem hospitals — and stays with you in your own language, every step of the way.
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