Overview
Tugba Kalayci practices in Istanbul, Turkey. Kalayci is rated as an Experienced expert by MediFind in the treatment of Trichothiodystrophy. Their top areas of expertise are Aarskog Syndrome, Ring Chromosome 13, Fetal Akinesia Sequence, and Brachyolmia.
Their clinical research consists of co-authoring 35 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, they have co-authored 1 article in the study of Trichothiodystrophy.
Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts 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.
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
- Advanced
- Aarskog SyndromeKalayci isAdvanced. Learn about Aarskog Syndrome.
- BrachyolmiaKalayci isAdvanced. Learn about Brachyolmia.
- Fetal Akinesia SequenceKalayci isAdvanced. Learn about Fetal Akinesia Sequence.
- Focal or Multifocal Malformations in Neuronal Migration
- MicrognathiaKalayci isAdvanced. Learn about Micrognathia.
- Ring Chromosome 13Kalayci isAdvanced. Learn about Ring Chromosome 13.
- Experienced
- 15q11.2 MicrodeletionKalayci isExperienced. Learn about 15q11.2 Microdeletion.
- Achalasia Microcephaly SyndromeKalayci isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Acromesomelic DysplasiaKalayci isExperienced. Learn about Acromesomelic Dysplasia.
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson Type
- Acromesomelic Dysplasia Maroteaux Type