Overview
Faiqa Imtiaz practices practicing medicine in Riyadh, Saudi Arabia.
Imtiaz is highly rated in 21 conditions, according to our data. Their clinical expertise encompasses Camptodactyly Taurinuria, Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia, Camptodactyly Syndrome Guadalajara Type 1, and Camptodactyly Syndrome Guadalajara Type 2.
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 Faiqa Imtiaz
Is Faiqa Imtiaz a top-rated expert for Camptodactyly Taurinuria?
MediFind is an objective health platform that identifies experts based on real-world data. Faiqa Imtiaz is classified as an Distinguished expert for Camptodactyly Taurinuria, 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 Faiqa Imtiaz participate in research or clinical trials?
Yes. Faiqa Imtiaz has published 56 articles and abstracts on conditions like Camptodactyly Taurinuria. You can view a list of Faiqa Imtiaz'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
- Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia
- Camptodactyly Syndrome Guadalajara Type 1
- Camptodactyly Syndrome Guadalajara Type 2
- Camptodactyly TaurinuriaImtiaz isDistinguished. Learn about Camptodactyly Taurinuria.
- Advanced
- Bilateral Renal Agenesis Dominant Type
- Cardiomyopathy Hypogonadism Metabolic Anomalies
- Deafness Craniofacial Syndrome
- Glucose-Galactose Malabsorption Deficiency
- Hearing LossImtiaz isAdvanced. Learn about Hearing Loss.
- Laron SyndromeImtiaz isAdvanced. Learn about Laron Syndrome.
- Maple Syrup Urine DiseaseImtiaz isAdvanced. Learn about Maple Syrup Urine Disease.
- Marden Walker Like Syndrome
- Marden-Walker SyndromeImtiaz isAdvanced. Learn about Marden-Walker Syndrome.
- Marshall SyndromeImtiaz isAdvanced. Learn about Marshall Syndrome.
- Nonsyndromic Hearing LossImtiaz isAdvanced. Learn about Nonsyndromic Hearing Loss.
- Potter SyndromeImtiaz isAdvanced. Learn about Potter Syndrome.
- Pyruvate Carboxylase Deficiency
- Retinitis PigmentosaImtiaz isAdvanced. Learn about Retinitis Pigmentosa.
- Retinopathy Pigmentary Mental Retardation
- Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
- Usher SyndromeImtiaz isAdvanced. Learn about Usher Syndrome.
- Experienced
- Achard SyndromeImtiaz isExperienced. Learn about Achard Syndrome.
- AcheiropodyImtiaz isExperienced. Learn about Acheiropody.
- Apolipoprotein C2 DeficiencyImtiaz isExperienced. Learn about Apolipoprotein C2 Deficiency.
- ArachnodactylyImtiaz isExperienced. Learn about Arachnodactyly.
- Argininosuccinic AciduriaImtiaz isExperienced. Learn about Argininosuccinic Aciduria.
- Bernard-Soulier SyndromeImtiaz isExperienced. Learn about Bernard-Soulier Syndrome.
- BlepharophimosisImtiaz isExperienced. Learn about Blepharophimosis.
- Blood ClotsImtiaz isExperienced. Learn about Blood Clots.
- Brachydactyly Mononen TypeImtiaz isExperienced. Learn about Brachydactyly Mononen Type.
- Cardiomyopathic LentiginosisImtiaz isExperienced. Learn about Cardiomyopathic Lentiginosis.
- Childhood PancreatitisImtiaz isExperienced. Learn about Childhood Pancreatitis.
- ChondrodystrophyImtiaz isExperienced. Learn about Chondrodystrophy.
- Enlarged LiverImtiaz isExperienced. Learn about Enlarged Liver.
- Factor 5 DeficiencyImtiaz isExperienced. Learn about Factor 5 Deficiency.
- Familial HypopituitarismImtiaz isExperienced. Learn about Familial Hypopituitarism.
- Familial Lipoprotein Lipase Deficiency
- FibrochondrogenesisImtiaz isExperienced. Learn about Fibrochondrogenesis.
- Flat FeetImtiaz isExperienced. Learn about Flat Feet.
- Fountain SyndromeImtiaz isExperienced. Learn about Fountain Syndrome.
- HemochromatosisImtiaz isExperienced. Learn about Hemochromatosis.
- HypopituitarismImtiaz isExperienced. Learn about Hypopituitarism.
- Infant Hearing LossImtiaz isExperienced. Learn about Infant Hearing Loss.
- Late-Onset Retinal DegenerationImtiaz isExperienced. Learn about Late-Onset Retinal Degeneration.
- MalnutritionImtiaz isExperienced. Learn about Malnutrition.
- MelasmaImtiaz isExperienced. Learn about Melasma.
- NephronophthisisImtiaz isExperienced. Learn about Nephronophthisis.
- PanhypopituitarismImtiaz isExperienced. Learn about Panhypopituitarism.
- Pendred SyndromeImtiaz isExperienced. Learn about Pendred Syndrome.
- Polycystic Kidney DiseaseImtiaz isExperienced. Learn about Polycystic Kidney Disease.
- Propionic AcidemiaImtiaz isExperienced. Learn about Propionic Acidemia.
- Pulmonary FibrosisImtiaz isExperienced. Learn about Pulmonary Fibrosis.
- Pulmonary Veno-Occlusive Disease
- PycnodysostosisImtiaz isExperienced. Learn about Pycnodysostosis.
- RicketsImtiaz isExperienced. Learn about Rickets.
- Schwartz-Jampel SyndromeImtiaz isExperienced. Learn about Schwartz-Jampel Syndrome.
- Sheehan SyndromeImtiaz isExperienced. Learn about Sheehan Syndrome.
- Spinocerebellar Ataxia Type 8Imtiaz isExperienced. Learn about Spinocerebellar Ataxia Type 8.
- Urea Cycle Disorders (UCD)Imtiaz isExperienced. Learn about Urea Cycle Disorders (UCD).
- Vitamin D DeficiencyImtiaz isExperienced. Learn about Vitamin D Deficiency.
- X-Linked HypophosphatemiaImtiaz isExperienced. Learn about X-Linked Hypophosphatemia.
- X-Linked Spondyloepiphyseal Dysplasia Tarda