Overview
Eduardo Perrone practices practicing medicine in Sao Paulo, Brazil.
Mr. Perrone is highly rated in 12 conditions, according to our data. His clinical expertise encompasses Gomez Lopez Hernandez Syndrome, Aplasia Cutis Congenita, Ectodermal Dysplasias, and Clouston Syndrome.
He is actively involved in clinical research, co-authoring 25 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 Eduardo Perrone
Is Eduardo Perrone a top-rated expert for Gomez Lopez Hernandez Syndrome?
MediFind is an objective health platform that identifies experts based on real-world data. Eduardo Perrone is classified as an Elite expert for Gomez Lopez Hernandez 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 Eduardo Perrone participate in research or clinical trials?
Yes. Eduardo Perrone has published 25 articles and abstracts on conditions like Gomez Lopez Hernandez Syndrome. You can view a list of Eduardo Perrone'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
- Elite
- Gomez Lopez Hernandez Syndrome
- Advanced
- Aplasia Cutis CongenitaMr. Perrone isAdvanced. Learn about Aplasia Cutis Congenita.
- Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia
- Camptodactyly Syndrome Guadalajara Type 1
- Camptodactyly Syndrome Guadalajara Type 2
- Camptodactyly TaurinuriaMr. Perrone isAdvanced. Learn about Camptodactyly Taurinuria.
- Clouston SyndromeMr. Perrone isAdvanced. Learn about Clouston Syndrome.
- Ectodermal DysplasiasMr. Perrone isAdvanced. Learn about Ectodermal Dysplasias.
- Gingival Fibromatosis with Hypertrichosis
- Keutel SyndromeMr. Perrone isAdvanced. Learn about Keutel Syndrome.
- Marden-Walker SyndromeMr. Perrone isAdvanced. Learn about Marden-Walker Syndrome.
- Neu Laxova SyndromeMr. Perrone isAdvanced. Learn about Neu Laxova Syndrome.
- Experienced
- 47 XYY SyndromeMr. Perrone isExperienced. Learn about 47 XYY Syndrome.
- Achard SyndromeMr. Perrone isExperienced. Learn about Achard Syndrome.
- AchondrogenesisMr. Perrone isExperienced. Learn about Achondrogenesis.
- Acromesomelic DysplasiaMr. Perrone isExperienced. Learn about Acromesomelic Dysplasia.
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson Type
- Acromesomelic Dysplasia Maroteaux TypeMr. Perrone isExperienced. Learn about Acromesomelic Dysplasia Maroteaux Type.
- Acromicric DysplasiaMr. Perrone isExperienced. Learn about Acromicric Dysplasia.
- ArachnodactylyMr. Perrone isExperienced. Learn about Arachnodactyly.
- Autosomal Recessive HypotrichosisMr. Perrone isExperienced. Learn about Autosomal Recessive Hypotrichosis.
- BlepharophimosisMr. Perrone isExperienced. Learn about Blepharophimosis.
- BowlegsMr. Perrone isExperienced. Learn about Bowlegs.
- BrachydactylyMr. Perrone isExperienced. Learn about Brachydactyly.
- Brachydactyly Mononen TypeMr. Perrone isExperienced. Learn about Brachydactyly Mononen Type.
- Caffey DiseaseMr. Perrone isExperienced. Learn about Caffey Disease.
- CherubismMr. Perrone isExperienced. Learn about Cherubism.
- ChondrodystrophyMr. Perrone isExperienced. Learn about Chondrodystrophy.
- Congenital AfibrinogenemiaMr. Perrone isExperienced. Learn about Congenital Afibrinogenemia.
- Cytochrome C Oxidase DeficiencyMr. Perrone isExperienced. Learn about Cytochrome C Oxidase Deficiency.
- Familial HypofibrinogenemiaMr. Perrone isExperienced. Learn about Familial Hypofibrinogenemia.
- Fibrous DysplasiaMr. Perrone isExperienced. Learn about Fibrous Dysplasia.
- Leigh SyndromeMr. Perrone isExperienced. Learn about Leigh Syndrome.
- MELAS SyndromeMr. Perrone isExperienced. Learn about MELAS Syndrome.
- MicrognathiaMr. Perrone isExperienced. Learn about Micrognathia.
- Nonsyndromic Hearing LossMr. Perrone isExperienced. Learn about Nonsyndromic Hearing Loss.
- Osteitis FibrosaMr. Perrone isExperienced. Learn about Osteitis Fibrosa.
- Primary Ciliary Dyskinesia (PCD)Mr. Perrone isExperienced. Learn about Primary Ciliary Dyskinesia (PCD).
- Schwartz-Jampel SyndromeMr. Perrone isExperienced. Learn about Schwartz-Jampel Syndrome.
- Spastic ParaparesisMr. Perrone isExperienced. Learn about Spastic Paraparesis.
- SpasticityMr. Perrone isExperienced. Learn about Spasticity.
- X-Linked Spondyloepiphyseal Dysplasia Tarda