Pediatric Genetic Diseases · Acibadem Altunizade Hospital, İstanbul Assoc. Prof. Özlem Akgün Doğan, MD
✓ Medically verified profileAssoc. Prof. Özlem Akgün Doğan, MD
Assoc. Prof. Özlem Akgün Doğan, MD is a specialist in Pediatric Genetic Diseases at Acibadem Altunizade Hospital in İstanbul. She evaluates and follows children with genetic conditions, with clinical interests in achondroplasia, Rett syndrome and Turner syndrome. Dr. Doğan consults in Turkish and English and offers video consultation for international patients.
Accepting international patientsAbout Assoc. Prof. Özlem Akgün Doğan, MD
Assoc. Prof. Özlem Akgün Doğan, MD is a specialist in Pediatric Genetic Diseases at Acibadem Altunizade Hospital in İstanbul. She has more than 20 years of experience in medicine and works with children and families affected by genetic conditions. Her clinical interests include achondroplasia, Rett syndrome and Turner syndrome.
Dr. Doğan graduated from Hacettepe University Faculty of Medicine in 2006. She completed her training in Child Health and Diseases at Dr. Sami Ulus Obstetrics and Gynecology, Child Health and Diseases Training and Research Hospital in 2011 and went on to complete training in Pediatric Genetic Diseases at Hacettepe University Faculty of Medicine in 2017. She has worked at Acıbadem Healthcare Services since 2021. She is a member of the Pediatric Genetic Diseases Association and the European Society of Human Genetics. Her published work includes co-authored studies on genetic panel screening and next-generation sequencing in monogenic systemic autoinflammatory diseases, clinical descriptions of rare conditions such as Peters Plus syndrome and H syndrome, rare chromosomal rearrangements, and SARS-CoV-2 sequencing and saliva-based testing in Istanbul.
Clinical focus
Dr. Doğan’s clinical work centers on the evaluation and follow-up of children with genetic conditions. In achondroplasia, a genetic condition affecting bone growth, her role includes assessing the clinical features, discussing genetic testing where appropriate and helping families understand the diagnosis. In Rett syndrome, a neurodevelopmental genetic condition, evaluation may involve reviewing the developmental history, considering genetic testing and coordinating with other pediatric specialists involved in the child’s care. In Turner syndrome, a chromosomal condition, assessment typically includes confirming the diagnosis through genetic testing and discussing which aspects of health may need monitoring over time.
Because a genetic diagnosis can affect several aspects of a child’s health, evaluation and follow-up may involve other pediatric specialties. Dr. Doğan discusses findings with families in a way that explains what a result does and does not mean, and outlines the options for further testing or follow-up. Each child’s situation is different, and recommendations depend on the individual clinical picture and the results available.
How Dr. Doğan works with international patients
Dr. Doğan consults in Turkish and English, and interpreters can be arranged for other languages. Before a visit, the Acibadem international patient team coordinates the collection of prior reports and imaging, such as genetic test results, laboratory results, X-ray or MRI reports, previous clinical assessments and discharge summaries, and arranges appointments and the hospital visit. A first consultation typically covers the child’s history and symptoms, a review of existing test results and previous treatments, a clinical examination and a discussion of the options. Video consultation is available for international patients and may be used for an initial discussion or to review existing reports before a family decides whether a visit to İstanbul is appropriate.
What Dr. Doğan treats and performs
Each item opens the condition or treatment page with the care pathway for international patients.
Conditions treated
Procedures performed
Education, career and memberships
Education & training
Education
- 2017Hacettepe University Faculty of Medicine Pediatric Genetic Diseases
- 2011Dr. Sami Ulus Obstetrics and Gynecology, Child Health and Diseases Training and Research Hospital Child Health and Diseases
- 2006Hacettepe University Faculty of Medicine
Career
Professional Experience
- 2021Acıbadem Healthcare Services
Memberships
Professional Memberships
- Pediatric Genetic Diseases Association
- European Society of Human Genetics
Selected publications
Selected Publications
- Comparison of the clinical diagnostic criteria and the results of the next-generation sequence gene panel in patients with monogenic systemic autoinflammatory diseases Clin Rheumatol. 2020 Nov 9. doi: 10.1007/sl0067-020-05492-8. Epub ahead of print. PMID: 33165748. Sözeri B, Demir F, Sönmez HE, Karadağ ŞG, Demirkol YK, Doğan ÖA, Doğanay HL, Ayaz NA.
- H syndrome with a novel homozygous SLC29A3 mutation in two sisters. Pediatr Dermatol. 2020 Nov;37(6): 1135-1138. doi: 10.1111/pde. 14322. Epub 2020 Aug 10.PMID: 32776596. Demir D, Aktaş Karabay E, Sözeri B, Gürsoy F, Akgün Doğan Ö, Topaktaş E, Zindancı İ.
- Does sampling saliva increase detection of SARS-CoV-2 by RT-PCR? Comparing saliva with oro-nasopharyngeal swabs J Virol Methods. 2020 Dec 30;290:114049. doi: 10.1016/j.jviromet.2020.114049. Epub ahead ofprint. PMID: 33387561; PMCID: PMC7833528. Dogan OA, Kose B, Agaoglu NB, Yildiz J, Alkurt G, Demirkol YK, Irvem A, Doganay GD, Doganay L.
- Peters Plus syndrome: a recognizable clinical entity. Türk J Pediatr. 2020;62(1): 136-140. doi: 10.24953/turkjped.2020.01.020. PMID: 32253880. Demir GÜ, Lafçı NG, Doğan ÖA, Şimşek-Kiper PÖ, Utine GE
- The origin of SARS-CoV-2 in Istanbul: Sequencing fmdings from the epicenter of the pandemic in Turkey. North Clin Istanb. 2020 May 15;7(3):203-209. doi: 10.14744/nci.2020.90532. PMID: 32478289; PMCID: PMC7251277. Karacan I, Akgun TK, Agaoglu NB, Irvem A, Alkurt G, Yildiz J, Kose B, Ozel AS, Altunal LN, Can ND, Demirkol YK, Aydin M, Dogan OA, Doganay L,DoganayGD
- Genetic panel screening in patients with clinically unclassified systemic autoinflammatory diseases Clin Rheumatol. 2020 Dec;39(12):3733-3745. doi: 10.1007/sl0067-020-05108-1. Epub 2020 May 26. PMID: 32458238 Demir F, Doğan ÖA, Demirkol YK, Tekkuş KE, Canbek S, Karadağ ŞG, Sönmez HE, Ayaz NA, Doğanay HL, Sözeri B
- Further Phenotypic Delineation of Partial Trisomy 17q and Partial Monosomy 20q due to Rare t(17;20) Mol Syndromol. 2020 Feb;ll(l):38-42. doi: 10.1159/000505141. Epub 2020 Jan 14. PMID: 32256300; PMCID: PMC7109379. Ürel-Demir G, Akgün-Doğan Ö, Oğuz S, Güleray-Lafcı N, Şimşek-Kiper PÖ, Eda Utine G, Alikaşifoğlu M, Boduroğlu K.
- Responding to COVID-19 in Istanbul: Perspective from genomic laboratory. North Clin Istanb. 2020 May 7;7(3):311-312. doi: 10.14744/nci.2020.30075. PMID: 32478308; PMCID: PMC7251262. Doganay L, Agaoglu NB, Irvem A, Alkurt G, Yildiz J, Köse B, Demirkol YK, Dogan OA, Doganay GD.
- The musculoskeletal system manifestations in children with familial Mediterranean fever. North Clin Istanb. 2020 Sep 4;7(5):438-442. doi: 10.14744/nci.2020.96636. PMID: 33163878; PMCID: PMC7603850. Demir F, Bolac GL, Merter T, Canbek S, Dogan OA, Demirkol YK, Yildiz J, Doganay HL, Sozeri B.
- Cafe noir spots: a feature of familial progressive hyper- and hypopigmentation J Eur Acad Dermatol Venereol. 2020 Feb;34(2):e76-e77. doi: 10.1111/jdv. 15968. Epub 2019 Oct 24. PMID: 31571311. Gülseren D, Güleray N, Akgün-Doğan Ö, Şimşek-Kiper PÖ, Utine EG, Alikaşifoğlu M, Ersoy-Evans S

