Overview
Fathiya Murshedi-Al practices practicing medicine in Muscat, Oman.
Murshedi-Al is highly rated in 2 conditions, according to our data. Their clinical expertise encompasses Hydranencephaly, Cytochrome C Oxidase Deficiency, Urea Cycle Disorders (UCD), and Retinopathy Pigmentary Mental Retardation.
They are actively involved in clinical research, co-authoring 37 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 Fathiya M. Murshedi-Al
Is Fathiya M. Murshedi-Al a top-rated expert for Hydranencephaly?
MediFind is an objective health platform that identifies experts based on real-world data. Fathiya M. Murshedi-Al is classified as an Advanced expert for Hydranencephaly, 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 Fathiya M. Murshedi-Al participate in research or clinical trials?
Yes. Fathiya M. Murshedi-Al has published 37 articles and abstracts on conditions like Hydranencephaly. You can view a list of Fathiya M. Murshedi-Al'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
- Cytochrome C Oxidase DeficiencyMurshedi-Al isAdvanced. Learn about Cytochrome C Oxidase Deficiency.
- HydranencephalyMurshedi-Al isAdvanced. Learn about Hydranencephaly.
- Experienced
- Achalasia Microcephaly SyndromeMurshedi-Al isExperienced. Learn about Achalasia Microcephaly Syndrome.
- CACH SyndromeMurshedi-Al isExperienced. Learn about CACH Syndrome.
- CitrullinemiaMurshedi-Al isExperienced. Learn about Citrullinemia.
- Cortical DysplasiaMurshedi-Al isExperienced. Learn about Cortical Dysplasia.
- Generalized Tonic-Clonic SeizureMurshedi-Al isExperienced. Learn about Generalized Tonic-Clonic Seizure.
- Hereditary Spastic ParaparesisMurshedi-Al isExperienced. Learn about Hereditary Spastic Paraparesis.
- HypotoniaMurshedi-Al isExperienced. Learn about Hypotonia.
- Lactic AcidosisMurshedi-Al isExperienced. Learn about Lactic Acidosis.
- Low Blood SugarMurshedi-Al isExperienced. Learn about Low Blood Sugar.
- Low Sodium LevelMurshedi-Al isExperienced. Learn about Low Sodium Level.
- Maple Syrup Urine DiseaseMurshedi-Al isExperienced. Learn about Maple Syrup Urine Disease.
- Metabolic AcidosisMurshedi-Al isExperienced. Learn about Metabolic Acidosis.
- Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1)
- Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD2)
- MicrocephalyMurshedi-Al isExperienced. Learn about Microcephaly.
- Newborn Low Blood SugarMurshedi-Al isExperienced. Learn about Newborn Low Blood Sugar.
- PEPCK 1 DeficiencyMurshedi-Al isExperienced. Learn about PEPCK 1 Deficiency.
- PorphyriaMurshedi-Al isExperienced. Learn about Porphyria.
- Propionic AcidemiaMurshedi-Al isExperienced. Learn about Propionic Acidemia.
- Retinopathy Pigmentary Mental RetardationMurshedi-Al isExperienced. Learn about Retinopathy Pigmentary Mental Retardation.
- SeizuresMurshedi-Al isExperienced. Learn about Seizures.
- Spastic Paraplegia Type 2Murshedi-Al isExperienced. Learn about Spastic Paraplegia Type 2.
- Spastic Paraplegia Type 7Murshedi-Al isExperienced. Learn about Spastic Paraplegia Type 7.
- SpasticityMurshedi-Al isExperienced. Learn about Spasticity.
- Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH)
- Urea Cycle Disorders (UCD)Murshedi-Al isExperienced. Learn about Urea Cycle Disorders (UCD).
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency