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Home Doctors Assoc. Prof. Dr. Ayşe Ergül Bozacı, MD
PEDIATRIC METABOLIC DISEASES · AKDENIZ UNIVERSITY HOSPITAL

Assoc. Prof. Dr. Ayşe Ergül Bozacı, MD

Associate Professor of Pediatrics — Head of Pediatric Metabolic Diseases · Akdeniz University Hospital
Assoc. Prof. Dr. Ayşe Ergül Bozacı heads the Pediatric Metabolic Diseases unit at Akdeniz University Hospital. She earned her MD at Akdeniz University (2008), completed her Pediatric Health and Diseases specialisation at the University of Health Sciences (2013) and her Pediatric Metabolic Diseases subspecialty fellowship at Ege University (2020). Her clinical and research focus is on inborn errors of metabolism, lysosomal storage disorders (MPS, Pompe disease), tyrosinemia, glutaric aciduria and other organic acidurias and mitochondrial disorders.
Specialties: Paediatrics
15+
years in pediatrics
5+
years in pediatric metabolic diseases
Inborn Errors of MetabolismLysosomal Storage DisordersPompe DiseaseMucopolysaccharidosesTyrosinemia
A BergemHealth coordinator arranges contact with the professor within 24–48 hours on business days.
Direct contract with BergemHealth
CONSULTATION LANGUAGES
TR Turkish · native
EN English · advanced
RU Russian · via BergemHealth coordinator
UK Ukrainian · via BergemHealth coordinator
AM
ANTALYA · 06/2026
EDUCATION & CAREER

Timeline

Career milestones.

2002-2008
MD (Undergraduate)
Akdeniz University Faculty of Medicine, Antalya
2009-2013
Specialization in Pediatric Health and Diseases (thesis on serum 25-OH vitamin D and zinc levels in children with asthma)
University of Health Sciences, Turkey
2016-2020
Subspecialty (Yan Dal) Expertise — Pediatric Metabolic Diseases
Ege University, İzmir
PUBLICATIONS

Scientific work

Selected peer-reviewed publications.

  • 2024
    Molecular Genetics and Metabolism Reports
    «The evaluation of inherited metabolic diseases presenting with rhabdomyolysis»
    · first author
  • 2024
    Molecular Syndromology
    «Mitochondrial DNA Depletion Syndromes Gene Panel versus Clinical Exome Sequencing»
    · co-author
  • 2023
    Molecular Genetics and Metabolism Reports
    «Glutaric aciduria and L-2-hydroxyglutaric aciduria: Clinical and molecular findings of 35 patients»
    · first author
  • 2022
    Journal of Pediatric Endocrinology and Metabolism
    «Long-term follow-up of alkaptonuria patients: Single center experience»
    · first author
  • 2022
    Life
    «Three-Country Snapshot of Ornithine Transcarbamylase Deficiency»
    · co-author
  • 2022
    Journal of Clinical Densitometry
    «Radiographic Findings of Mucopolysaccharidosis and Comparison with Bone Mineral Density»
    · first author
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