Overview
Egle Preiksaitiene practices practicing medicine in Vilnius, Lithuania.
Preiksaitiene is highly rated in 7 conditions, according to our data. Their clinical expertise encompasses CHARGE Syndrome, Greig Cephalopolysyndactyly Syndrome, Chromosome 4q Deletion, Micrognathia, and Tissue Biopsy.
They are actively involved in clinical research, co-authoring 56 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 Egle Preiksaitiene
Is Egle Preiksaitiene a top-rated expert for CHARGE Syndrome?
MediFind is an objective health platform that identifies experts based on real-world data. Egle Preiksaitiene is classified as an Distinguished expert for CHARGE Syndrome, 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 Egle Preiksaitiene participate in research or clinical trials?
Yes. Egle Preiksaitiene has published 56 articles and abstracts on conditions like CHARGE Syndrome. You can view a list of Egle Preiksaitiene'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
- CHARGE SyndromePreiksaitiene isDistinguished. Learn about CHARGE Syndrome.
- Advanced
- BlepharophimosisPreiksaitiene isAdvanced. Learn about Blepharophimosis.
- Chromosome 4q DeletionPreiksaitiene isAdvanced. Learn about Chromosome 4q Deletion.
- Feingold SyndromePreiksaitiene isAdvanced. Learn about Feingold Syndrome.
- Greig Cephalopolysyndactyly SyndromePreiksaitiene isAdvanced. Learn about Greig Cephalopolysyndactyly Syndrome.
- MicrognathiaPreiksaitiene isAdvanced. Learn about Micrognathia.
- Partial Androgen Insensitivity Syndrome (PAIS)
- Experienced
- Achalasia Microcephaly SyndromePreiksaitiene isExperienced. Learn about Achalasia Microcephaly Syndrome.
- AcrocephalopolydactylyPreiksaitiene isExperienced. Learn about Acrocephalopolydactyly.
- AcrodysostosisPreiksaitiene isExperienced. Learn about Acrodysostosis.
- Acromicric DysplasiaPreiksaitiene isExperienced. Learn about Acromicric Dysplasia.
- Aicardi-Goutieres SyndromePreiksaitiene isExperienced. Learn about Aicardi-Goutieres Syndrome.
- AlbinismPreiksaitiene isExperienced. Learn about Albinism.
- Apert SyndromePreiksaitiene isExperienced. Learn about Apert Syndrome.
- ArrhythmiasPreiksaitiene isExperienced. Learn about Arrhythmias.
- Arthrogryposis Multiplex CongenitaPreiksaitiene isExperienced. Learn about Arthrogryposis Multiplex Congenita.
- Axenfeld-Rieger SyndromePreiksaitiene isExperienced. Learn about Axenfeld-Rieger Syndrome.
- Brachydactyly Mononen TypePreiksaitiene isExperienced. Learn about Brachydactyly Mononen Type.
- Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia
- Camptodactyly Syndrome Guadalajara Type 1Preiksaitiene isExperienced. Learn about Camptodactyly Syndrome Guadalajara Type 1.
- Camptodactyly Syndrome Guadalajara Type 2Preiksaitiene isExperienced. Learn about Camptodactyly Syndrome Guadalajara Type 2.
- Camptodactyly TaurinuriaPreiksaitiene isExperienced. Learn about Camptodactyly Taurinuria.
- Cardiac ArrestPreiksaitiene isExperienced. Learn about Cardiac Arrest.
- CardiomyopathyPreiksaitiene isExperienced. Learn about Cardiomyopathy.
- Choanal AtresiaPreiksaitiene isExperienced. Learn about Choanal Atresia.
- ChondrodystrophyPreiksaitiene isExperienced. Learn about Chondrodystrophy.
- Chromosome 3q DuplicationPreiksaitiene isExperienced. Learn about Chromosome 3q Duplication.
- Chromosome 7p DuplicationPreiksaitiene isExperienced. Learn about Chromosome 7p Duplication.
- ClubfootPreiksaitiene isExperienced. Learn about Clubfoot.
- Coffin-Siris SyndromePreiksaitiene isExperienced. Learn about Coffin-Siris Syndrome.
- Congenital ContracturesPreiksaitiene isExperienced. Learn about Congenital Contractures.
- Congenital Radioulnar SynostosisPreiksaitiene isExperienced. Learn about Congenital Radioulnar Synostosis.
- Cortical DysplasiaPreiksaitiene isExperienced. Learn about Cortical Dysplasia.
- CraniosynostosisPreiksaitiene isExperienced. Learn about Craniosynostosis.
- Dandy-Walker SyndromePreiksaitiene isExperienced. Learn about Dandy-Walker Syndrome.
- Drug Induced DyskinesiaPreiksaitiene isExperienced. Learn about Drug Induced Dyskinesia.
- DysarthriaPreiksaitiene isExperienced. Learn about Dysarthria.
- Dysostosis PeripheralPreiksaitiene isExperienced. Learn about Dysostosis Peripheral.
- Familial Ventricular TachycardiaPreiksaitiene isExperienced. Learn about Familial Ventricular Tachycardia.
- Hereditary Multiple OsteochondromasPreiksaitiene isExperienced. Learn about Hereditary Multiple Osteochondromas.
- Hypertrophic Cardiomyopathy (HCM)Preiksaitiene isExperienced. Learn about Hypertrophic Cardiomyopathy (HCM).
- HypotoniaPreiksaitiene isExperienced. Learn about Hypotonia.
- IntersexPreiksaitiene isExperienced. Learn about Intersex.
- Iridogoniodysgenesis Type 1Preiksaitiene isExperienced. Learn about Iridogoniodysgenesis Type 1.
- Limb-Girdle Muscular DystrophyPreiksaitiene isExperienced. Learn about Limb-Girdle Muscular Dystrophy.
- Long QT SyndromePreiksaitiene isExperienced. Learn about Long QT Syndrome.
- Long QT Syndrome 2Preiksaitiene isExperienced. Learn about Long QT Syndrome 2.
- Metopic RidgePreiksaitiene isExperienced. Learn about Metopic Ridge.
- Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1)
- Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD2)
- MicrocephalyPreiksaitiene isExperienced. Learn about Microcephaly.
- Miller SyndromePreiksaitiene isExperienced. Learn about Miller Syndrome.
- OmphalocelePreiksaitiene isExperienced. Learn about Omphalocele.
- OsteochondromaPreiksaitiene isExperienced. Learn about Osteochondroma.
- Pfeiffer SyndromePreiksaitiene isExperienced. Learn about Pfeiffer Syndrome.
- PiebaldismPreiksaitiene isExperienced. Learn about Piebaldism.
- PlagiocephalyPreiksaitiene isExperienced. Learn about Plagiocephaly.
- Primary AmyloidosisPreiksaitiene isExperienced. Learn about Primary Amyloidosis.
- Saethre-Chotzen SyndromePreiksaitiene isExperienced. Learn about Saethre-Chotzen Syndrome.
- Schwartz-Jampel SyndromePreiksaitiene isExperienced. Learn about Schwartz-Jampel Syndrome.
- Swyer SyndromePreiksaitiene isExperienced. Learn about Swyer Syndrome.
- SyndactylyPreiksaitiene isExperienced. Learn about Syndactyly.
- Tissue BiopsyPreiksaitiene isExperienced. Learn about Tissue Biopsy.
- Tracheoesophageal FistulaPreiksaitiene isExperienced. Learn about Tracheoesophageal Fistula.
- Transthyretin AmyloidosisPreiksaitiene isExperienced. Learn about Transthyretin Amyloidosis.
- Turner SyndromePreiksaitiene isExperienced. Learn about Turner Syndrome.
- Umbilical HerniaPreiksaitiene isExperienced. Learn about Umbilical Hernia.
- Van Maldergem SyndromePreiksaitiene isExperienced. Learn about Van Maldergem Syndrome.
- Ventricular TachycardiaPreiksaitiene isExperienced. Learn about Ventricular Tachycardia.
- Werner SyndromePreiksaitiene isExperienced. Learn about Werner Syndrome.
- X-Linked Spondyloepiphyseal Dysplasia TardaPreiksaitiene isExperienced. Learn about X-Linked Spondyloepiphyseal Dysplasia Tarda.