Overview
Katrin Ounap practices practicing medicine in Tartu, Estonia.
Ms. Ounap is highly rated in 33 conditions, according to our data. Her clinical expertise encompasses Hypotonia, Beckwith-Wiedemann Syndrome, Classic Galactosemia, and Macroglossia.
She is actively involved in clinical research, co-authoring 176 peer reviewed articles.
Gender
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 Katrin Ounap
Is Katrin Ounap a top-rated expert for Hypotonia?
MediFind is an objective health platform that identifies experts based on real-world data. Katrin Ounap is classified as an Distinguished expert for Hypotonia, 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 Katrin Ounap participate in research or clinical trials?
Yes. Katrin Ounap has published 174 articles and abstracts on conditions like Hypotonia. You can view a list of Katrin Ounap'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
- Distinguished
- Beckwith-Wiedemann SyndromeMs. Ounap isDistinguished. Learn about Beckwith-Wiedemann Syndrome.
- Classic GalactosemiaMs. Ounap isDistinguished. Learn about Classic Galactosemia.
- Cortical DysplasiaMs. Ounap isDistinguished. Learn about Cortical Dysplasia.
- HypotoniaMs. Ounap isDistinguished. Learn about Hypotonia.
- MacroglossiaMs. Ounap isDistinguished. Learn about Macroglossia.
- Advanced
- Achalasia Microcephaly SyndromeMs. Ounap isAdvanced. Learn about Achalasia Microcephaly Syndrome.
- Cerebellar HypoplasiaMs. Ounap isAdvanced. Learn about Cerebellar Hypoplasia.
- Dihydropteridine Reductase Deficiency
- Drug Induced DyskinesiaMs. Ounap isAdvanced. Learn about Drug Induced Dyskinesia.
- Dubowitz SyndromeMs. Ounap isAdvanced. Learn about Dubowitz Syndrome.
- EpilepsyMs. Ounap isAdvanced. Learn about Epilepsy.
- Epilepsy in ChildrenMs. Ounap isAdvanced. Learn about Epilepsy in Children.
- Floating-Harbor SyndromeMs. Ounap isAdvanced. Learn about Floating-Harbor Syndrome.
- Galactokinase DeficiencyMs. Ounap isAdvanced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMs. Ounap isAdvanced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMs. Ounap isAdvanced. Learn about Galactosemia.
- GigantismMs. Ounap isAdvanced. Learn about Gigantism.
- Increased Head CircumferenceMs. Ounap isAdvanced. Learn about Increased Head Circumference.
- KBG SyndromeMs. Ounap isAdvanced. Learn about KBG Syndrome.
- MicrocephalyMs. Ounap isAdvanced. Learn about Microcephaly.
- Mitochondrial Complex 1 Deficiency
- Multiple Synostoses Syndrome 1Ms. Ounap isAdvanced. Learn about Multiple Synostoses Syndrome 1.
- PEHO SyndromeMs. Ounap isAdvanced. Learn about PEHO Syndrome.
- Phenylketonuria (PKU)Ms. Ounap isAdvanced. Learn about Phenylketonuria (PKU).
- PMM2-Congenital Disorder of Glycosylation
- Primary Lateral SclerosisMs. Ounap isAdvanced. Learn about Primary Lateral Sclerosis.
- Pyruvate Decarboxylase Deficiency
- Pyruvate Dehydrogenase Deficiency
- Russell-Silver DwarfismMs. Ounap isAdvanced. Learn about Russell-Silver Dwarfism.
- SeizuresMs. Ounap isAdvanced. Learn about Seizures.
- Sotos SyndromeMs. Ounap isAdvanced. Learn about Sotos Syndrome.
- Trisomy 14 MosaicismMs. Ounap isAdvanced. Learn about Trisomy 14 Mosaicism.
- West SyndromeMs. Ounap isAdvanced. Learn about West Syndrome.
- Experienced
- Absence SeizureMs. Ounap isExperienced. Learn about Absence Seizure.
- Acute Cerebellar AtaxiaMs. Ounap isExperienced. Learn about Acute Cerebellar Ataxia.
- AgranulocytosisMs. Ounap isExperienced. Learn about Agranulocytosis.
- Angelman SyndromeMs. Ounap isExperienced. Learn about Angelman Syndrome.
- Arthrogryposis Multiplex CongenitaMs. Ounap isExperienced. Learn about Arthrogryposis Multiplex Congenita.
- AthetosisMs. Ounap isExperienced. Learn about Athetosis.
- Autism Spectrum DisorderMs. Ounap isExperienced. Learn about Autism Spectrum Disorder.
- Brachydactyly Mononen TypeMs. Ounap isExperienced. Learn about Brachydactyly Mononen Type.
- CACH SyndromeMs. Ounap isExperienced. Learn about CACH Syndrome.
- CalcinosisMs. Ounap isExperienced. Learn about Calcinosis.
- CardiomyopathyMs. Ounap isExperienced. Learn about Cardiomyopathy.
- CataractMs. Ounap isExperienced. Learn about Cataract.
- Charcot-Marie-Tooth DiseaseMs. Ounap isExperienced. Learn about Charcot-Marie-Tooth Disease.
- ChondrodystrophyMs. Ounap isExperienced. Learn about Chondrodystrophy.
- ChoreaMs. Ounap isExperienced. Learn about Chorea.
- Coffin-Lowry SyndromeMs. Ounap isExperienced. Learn about Coffin-Lowry Syndrome.
- Congenital ContracturesMs. Ounap isExperienced. Learn about Congenital Contractures.
- Congenital HypothyroidismMs. Ounap isExperienced. Learn about Congenital Hypothyroidism.
- Congenital Myasthenic SyndromeMs. Ounap isExperienced. Learn about Congenital Myasthenic Syndrome.
- Delayed GrowthMs. Ounap isExperienced. Learn about Delayed Growth.
- Dihydrolipoamide Dehydrogenase Deficiency
- DysarthriaMs. Ounap isExperienced. Learn about Dysarthria.
- Early Infantile Epileptic Encephalopathy
- EncephaloceleMs. Ounap isExperienced. Learn about Encephalocele.
- Epilepsy with Myoclonic-Atonic Seizures
- Familial Colorectal CancerMs. Ounap isExperienced. Learn about Familial Colorectal Cancer.
- Familial PorencephalyMs. Ounap isExperienced. Learn about Familial Porencephaly.
- Generalized Tonic-Clonic SeizureMs. Ounap isExperienced. Learn about Generalized Tonic-Clonic Seizure.
- Glutaric Acidemia Type 2Ms. Ounap isExperienced. Learn about Glutaric Acidemia Type 2.
- Hearing LossMs. Ounap isExperienced. Learn about Hearing Loss.
- HemihyperplasiaMs. Ounap isExperienced. Learn about Hemihyperplasia.
- Hereditary HyperekplexiaMs. Ounap isExperienced. Learn about Hereditary Hyperekplexia.
- HerniaMs. Ounap isExperienced. Learn about Hernia.
- Infant Respiratory Distress SyndromeMs. Ounap isExperienced. Learn about Infant Respiratory Distress Syndrome.
- Infantile NeutropeniaMs. Ounap isExperienced. Learn about Infantile Neutropenia.
- Intrauterine Growth RestrictionMs. Ounap isExperienced. Learn about Intrauterine Growth Restriction.
- Juvenile Polyposis SyndromeMs. Ounap isExperienced. Learn about Juvenile Polyposis Syndrome.
- Knobloch SyndromeMs. Ounap isExperienced. Learn about Knobloch Syndrome.
- Leber Hereditary Optic Neuropathy (LHON)
- Leigh SyndromeMs. Ounap isExperienced. Learn about Leigh Syndrome.
- LeukodystrophyMs. Ounap isExperienced. Learn about Leukodystrophy.
- Limb-Girdle Muscular DystrophyMs. Ounap isExperienced. Learn about Limb-Girdle Muscular Dystrophy.
- Lynch SyndromeMs. Ounap isExperienced. Learn about Lynch Syndrome.
- Meckel SyndromeMs. Ounap isExperienced. Learn about Meckel Syndrome.
- Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1)
- Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD2)
- Microcephaly Deafness SyndromeMs. Ounap isExperienced. Learn about Microcephaly Deafness Syndrome.
- MigraineMs. Ounap isExperienced. Learn about Migraine.
- MosaicismMs. Ounap isExperienced. Learn about Mosaicism.
- Movement DisordersMs. Ounap isExperienced. Learn about Movement Disorders.
- Mucopolysaccharidoses (MPS)Ms. Ounap isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Muscle AtrophyMs. Ounap isExperienced. Learn about Muscle Atrophy.
- Myoclonic EpilepsyMs. Ounap isExperienced. Learn about Myoclonic Epilepsy.
- Olivopontocerebellar AtrophyMs. Ounap isExperienced. Learn about Olivopontocerebellar Atrophy.
- Optic Nerve AtrophyMs. Ounap isExperienced. Learn about Optic Nerve Atrophy.
- Ovarian CancerMs. Ounap isExperienced. Learn about Ovarian Cancer.
- Pectus ExcavatumMs. Ounap isExperienced. Learn about Pectus Excavatum.
- Periventricular HeterotopiaMs. Ounap isExperienced. Learn about Periventricular Heterotopia.
- PorencephalyMs. Ounap isExperienced. Learn about Porencephaly.
- Prader-Willi SyndromeMs. Ounap isExperienced. Learn about Prader-Willi Syndrome.
- Premature Ovarian FailureMs. Ounap isExperienced. Learn about Premature Ovarian Failure.
- Schwartz-Jampel SyndromeMs. Ounap isExperienced. Learn about Schwartz-Jampel Syndrome.
- Short PhiltrumMs. Ounap isExperienced. Learn about Short Philtrum.
- Sideroblastic AnemiaMs. Ounap isExperienced. Learn about Sideroblastic Anemia.
- Simpson-Golabi-Behmel SyndromeMs. Ounap isExperienced. Learn about Simpson-Golabi-Behmel Syndrome.
- Spasmus NutansMs. Ounap isExperienced. Learn about Spasmus Nutans.
- SpasticityMs. Ounap isExperienced. Learn about Spasticity.
- Spinal Muscular Atrophy (SMA)Ms. Ounap isExperienced. Learn about Spinal Muscular Atrophy (SMA).
- Spinocerebellar AtaxiaMs. Ounap isExperienced. Learn about Spinocerebellar Ataxia.
- Spondylocostal DysostosisMs. Ounap isExperienced. Learn about Spondylocostal Dysostosis.
- Spondyloepimetaphyseal Dysplasia Strudwick Type
- Temple SyndromeMs. Ounap isExperienced. Learn about Temple Syndrome.
- Ventricular Septal DefectsMs. Ounap isExperienced. Learn about Ventricular Septal Defects.
- Vitamin B12 Deficiency AnemiaMs. Ounap isExperienced. Learn about Vitamin B12 Deficiency Anemia.
- Weaver SyndromeMs. Ounap isExperienced. Learn about Weaver Syndrome.
- Wolf-Hirschhorn SyndromeMs. Ounap isExperienced. Learn about Wolf-Hirschhorn Syndrome.
- X-Linked Creatine DeficiencyMs. Ounap isExperienced. Learn about X-Linked Creatine Deficiency.
- X-Linked Spondyloepiphyseal Dysplasia Tarda