Overview
Myrthe Van Den Born practices practicing medicine in Rotterdam, Netherlands.
Van Den Born is highly rated in 4 conditions, according to our data. Their clinical expertise encompasses Micrognathia, Chromosome 13q Duplication, Trisomy 13, and Coffin-Siris Syndrome.
They are actively involved in clinical research, co-authoring 26 peer reviewed articles.
Locations
Rotterdam, ZH, Netherlands
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 Myrthe A. Van Den Born
Is Myrthe A. Van Den Born a top-rated expert for Micrognathia?
MediFind is an objective health platform that identifies experts based on real-world data. Myrthe A. Van Den Born is classified as an Advanced expert for Micrognathia, 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 Myrthe A. Van Den Born participate in research or clinical trials?
Yes. Myrthe A. Van Den Born has published 26 articles and abstracts on conditions like Micrognathia. You can view a list of Myrthe A. Van Den Born'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
- Chromosome 13q DuplicationVan Den Born isAdvanced. Learn about Chromosome 13q Duplication.
- Coffin-Siris SyndromeVan Den Born isAdvanced. Learn about Coffin-Siris Syndrome.
- MicrognathiaVan Den Born isAdvanced. Learn about Micrognathia.
- Trisomy 13Van Den Born isAdvanced. Learn about Trisomy 13.
- Experienced
- Acromesomelic DysplasiaVan Den Born isExperienced. Learn about Acromesomelic Dysplasia.
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson Type
- Acromesomelic Dysplasia Maroteaux TypeVan Den Born isExperienced. Learn about Acromesomelic Dysplasia Maroteaux Type.
- ArthritisVan Den Born isExperienced. Learn about Arthritis.
- Brachydactyly Mononen TypeVan Den Born isExperienced. Learn about Brachydactyly Mononen Type.
- ChondrodystrophyVan Den Born isExperienced. Learn about Chondrodystrophy.
- Chromosome 16 TrisomyVan Den Born isExperienced. Learn about Chromosome 16 Trisomy.
- Glucose Phosphate Isomerase DeficiencyVan Den Born isExperienced. Learn about Glucose Phosphate Isomerase Deficiency.
- Marfan SyndromeVan Den Born isExperienced. Learn about Marfan Syndrome.
- Miller SyndromeVan Den Born isExperienced. Learn about Miller Syndrome.
- MosaicismVan Den Born isExperienced. Learn about Mosaicism.
- N-Acetylglutamate Synthase DeficiencyVan Den Born isExperienced. Learn about N-Acetylglutamate Synthase Deficiency.
- OsteoarthritisVan Den Born isExperienced. Learn about Osteoarthritis.
- Schwartz-Jampel SyndromeVan Den Born isExperienced. Learn about Schwartz-Jampel Syndrome.
- Trisomy 18Van Den Born isExperienced. Learn about Trisomy 18.
- Urea Cycle Disorders (UCD)Van Den Born isExperienced. Learn about Urea Cycle Disorders (UCD).
- X-Linked Spondyloepiphyseal Dysplasia TardaVan Den Born isExperienced. Learn about X-Linked Spondyloepiphyseal Dysplasia Tarda.