Overview
Magdalena Pelc practices in Warsaw, Poland. Ms. Pelc is rated as a Distinguished expert by MediFind in the treatment of Beckwith-Wiedemann Syndrome. Her top areas of expertise are RASopathies, Macroglossia, Beckwith-Wiedemann Syndrome, and Noonan Syndrome.
Her clinical research consists of co-authoring 13 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of Beckwith-Wiedemann Syndrome.
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
- Distinguished
- Beckwith-Wiedemann SyndromeMs. Pelc isDistinguished. Learn about Beckwith-Wiedemann Syndrome.
- MacroglossiaMs. Pelc isDistinguished. Learn about Macroglossia.
- RASopathiesMs. Pelc isDistinguished. Learn about RASopathies.
- Advanced
- Costello SyndromeMs. Pelc isAdvanced. Learn about Costello Syndrome.
- Noonan SyndromeMs. Pelc isAdvanced. Learn about Noonan Syndrome.
- Rommen Mueller Sybert Syndrome
- Sandhaus Ben-Ami SyndromeMs. Pelc isAdvanced. Learn about Sandhaus Ben-Ami Syndrome.
- Experienced
- Alport SyndromeMs. Pelc isExperienced. Learn about Alport Syndrome.
- ArrhythmiasMs. Pelc isExperienced. Learn about Arrhythmias.
- BlepharophimosisMs. Pelc isExperienced. Learn about Blepharophimosis.
- Brain TumorMs. Pelc isExperienced. Learn about Brain Tumor.
- Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia
- Camptodactyly Syndrome Guadalajara Type 1