Overview
Altug Koc practices practicing medicine in Izmir, Turkey.
Koc is highly rated in 2 conditions, according to our data. Their clinical expertise encompasses Ring Chromosome 13, Bone Dysplasia Corpus Callosum Agenesis, Familial Mediterranean Fever, and Trisomy 13.
They are actively involved in clinical research, co-authoring 52 peer reviewed articles.
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.
Frequently Asked Questions about Altug Koc
Is Altug Koc a top-rated expert for Ring Chromosome 13?
MediFind is an objective health platform that identifies experts based on real-world data. Altug Koc is classified as an Advanced expert for Ring Chromosome 13, 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.
Does Altug Koc participate in research or clinical trials?
Yes. Altug Koc has published 52 articles and abstracts on conditions like Ring Chromosome 13. You can view a list of Altug Koc's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
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
- Bone Dysplasia Corpus Callosum Agenesis
- Ring Chromosome 13Koc isAdvanced. Learn about Ring Chromosome 13.
- Experienced
- Achalasia Microcephaly Syndrome
- Acromicric DysplasiaKoc isExperienced. Learn about Acromicric Dysplasia.
- Bartter SyndromeKoc isExperienced. Learn about Bartter Syndrome.
- Brachydactyly Mononen Type
- ChondrodystrophyKoc isExperienced. Learn about Chondrodystrophy.
- Chromosome 13q Duplication
- Corpus Callosum AgenesisKoc isExperienced. Learn about Corpus Callosum Agenesis.
- Cortical DysplasiaKoc isExperienced. Learn about Cortical Dysplasia.
- Crouzon SyndromeKoc isExperienced. Learn about Crouzon Syndrome.
- Down SyndromeKoc isExperienced. Learn about Down Syndrome.
- Familial Mediterranean Fever
- Flat FeetKoc isExperienced. Learn about Flat Feet.
- Gestational Trophoblastic Disease
- Hearing LossKoc isExperienced. Learn about Hearing Loss.
- Hydatidiform MoleKoc isExperienced. Learn about Hydatidiform Mole.
- HypercalcemiaKoc isExperienced. Learn about Hypercalcemia.
- HypothyroidismKoc isExperienced. Learn about Hypothyroidism.
- Immune Defect due to Absence of Thymus
- Increased Head Circumference
- Intrauterine Growth Restriction
- Intussusception in Children
- Lichen PlanusKoc isExperienced. Learn about Lichen Planus.
- Lung CancerKoc isExperienced. Learn about Lung Cancer.
- MelasmaKoc isExperienced. Learn about Melasma.
- MicrocephalyKoc isExperienced. Learn about Microcephaly.
- Microcephaly Deafness Syndrome
- Milk-Alkali SyndromeKoc isExperienced. Learn about Milk-Alkali Syndrome.
- NephrocalcinosisKoc isExperienced. Learn about Nephrocalcinosis.
- Non-Small Cell Lung Cancer (NSCLC)
- Peutz-Jeghers SyndromeKoc isExperienced. Learn about Peutz-Jeghers Syndrome.
- Placenta PreviaKoc isExperienced. Learn about Placenta Previa.
- PolyhydramniosKoc isExperienced. Learn about Polyhydramnios.
- PolymicrogyriaKoc isExperienced. Learn about Polymicrogyria.
- PtosisKoc isExperienced. Learn about Ptosis.
- Schwartz-Jampel SyndromeKoc isExperienced. Learn about Schwartz-Jampel Syndrome.
- Trisomy 13Koc isExperienced. Learn about Trisomy 13.
- Trisomy 18Koc isExperienced. Learn about Trisomy 18.
- X-Linked Spondyloepiphyseal Dysplasia Tarda