Overview
Neila Belguith practices practicing medicine in Sfax, Tunisia.
Ms. Belguith is highly rated in 8 conditions, according to our data. Her clinical expertise encompasses Intersex, Turner Syndrome, Thyroid Dysgenesis, and Trisomy 13.
She is actively involved in clinical research, co-authoring 34 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 Neila Belguith
Is Neila Belguith a top-rated expert for Intersex?
MediFind is an objective health platform that identifies experts based on real-world data. Neila Belguith is classified as an Distinguished expert for Intersex, 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 Neila Belguith participate in research or clinical trials?
Yes. Neila Belguith has published 34 articles and abstracts on conditions like Intersex. You can view a list of Neila Belguith'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
- IntersexMs. Belguith isDistinguished. Learn about Intersex.
- Advanced
- Chromosome 13q DuplicationMs. Belguith isAdvanced. Learn about Chromosome 13q Duplication.
- Congenital HypothyroidismMs. Belguith isAdvanced. Learn about Congenital Hypothyroidism.
- HypothyroidismMs. Belguith isAdvanced. Learn about Hypothyroidism.
- Peters Plus SyndromeMs. Belguith isAdvanced. Learn about Peters Plus Syndrome.
- Thyroid DysgenesisMs. Belguith isAdvanced. Learn about Thyroid Dysgenesis.
- Trisomy 13Ms. Belguith isAdvanced. Learn about Trisomy 13.
- Turner SyndromeMs. Belguith isAdvanced. Learn about Turner Syndrome.
- Experienced
- Adrenal Insufficiency PediatricMs. Belguith isExperienced. Learn about Adrenal Insufficiency Pediatric.
- Autosomal Dominant Polycystic Kidney Disease
- EpilepsyMs. Belguith isExperienced. Learn about Epilepsy.
- Familial Colorectal CancerMs. Belguith isExperienced. Learn about Familial Colorectal Cancer.
- Familial HypopituitarismMs. Belguith isExperienced. Learn about Familial Hypopituitarism.
- HypogonadismMs. Belguith isExperienced. Learn about Hypogonadism.
- Hypogonadotropic HypogonadismMs. Belguith isExperienced. Learn about Hypogonadotropic Hypogonadism.
- HypopituitarismMs. Belguith isExperienced. Learn about Hypopituitarism.
- Leydig Cell HypoplasiaMs. Belguith isExperienced. Learn about Leydig Cell Hypoplasia.
- Li-Fraumeni SyndromeMs. Belguith isExperienced. Learn about Li-Fraumeni Syndrome.
- Mosaic Trisomy 9Ms. Belguith isExperienced. Learn about Mosaic Trisomy 9.
- MosaicismMs. Belguith isExperienced. Learn about Mosaicism.
- NephronophthisisMs. Belguith isExperienced. Learn about Nephronophthisis.
- Polycystic Kidney DiseaseMs. Belguith isExperienced. Learn about Polycystic Kidney Disease.
- Sheehan SyndromeMs. Belguith isExperienced. Learn about Sheehan Syndrome.
- Spasmus NutansMs. Belguith isExperienced. Learn about Spasmus Nutans.
- West SyndromeMs. Belguith isExperienced. Learn about West Syndrome.
- Xeroderma PigmentosumMs. Belguith isExperienced. Learn about Xeroderma Pigmentosum.