Overview
Majid Alfadhel practices practicing medicine in Riyadh, Saudi Arabia.
Mr. Alfadhel is highly rated in 33 conditions, according to our data. His clinical expertise encompasses Polydactyly, Hypotonia, Achalasia Microcephaly Syndrome, and Microcephaly.
He is actively involved in clinical research, co-authoring 223 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 Majid Alfadhel
Is Majid Alfadhel a top-rated expert for Polydactyly?
MediFind is an objective health platform that identifies experts based on real-world data. Majid Alfadhel is classified as an Elite expert for Polydactyly, 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 Majid Alfadhel participate in research or clinical trials?
Yes. Majid Alfadhel has published 223 articles and abstracts on conditions like Polydactyly. You can view a list of Majid Alfadhel'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
- PolydactylyMr. Alfadhel isElite. Learn about Polydactyly.
- Distinguished
- Achalasia Microcephaly SyndromeMr. Alfadhel isDistinguished. Learn about Achalasia Microcephaly Syndrome.
- Cortical DysplasiaMr. Alfadhel isDistinguished. Learn about Cortical Dysplasia.
- HypotoniaMr. Alfadhel isDistinguished. Learn about Hypotonia.
- MicrocephalyMr. Alfadhel isDistinguished. Learn about Microcephaly.
- Microcephaly with Spastic QuadriplegiaMr. Alfadhel isDistinguished. Learn about Microcephaly with Spastic Quadriplegia.
- Propionic AcidemiaMr. Alfadhel isDistinguished. Learn about Propionic Acidemia.
- Advanced
- Acute Cerebellar AtaxiaMr. Alfadhel isAdvanced. Learn about Acute Cerebellar Ataxia.
- ALG9-CDGMr. Alfadhel isAdvanced. Learn about ALG9-CDG.
- Aromatic L-Amino Acid Decarboxylase (AADC) Deficiency
- Biliary HypoplasiaMr. Alfadhel isAdvanced. Learn about Biliary Hypoplasia.
- CACH SyndromeMr. Alfadhel isAdvanced. Learn about CACH Syndrome.
- Cholesteryl Ester Storage DiseaseMr. Alfadhel isAdvanced. Learn about Cholesteryl Ester Storage Disease.
- Congenital Generalized LipodystrophyMr. Alfadhel isAdvanced. Learn about Congenital Generalized Lipodystrophy.
- CystinuriaMr. Alfadhel isAdvanced. Learn about Cystinuria.
- Drug Induced DyskinesiaMr. Alfadhel isAdvanced. Learn about Drug Induced Dyskinesia.
- DysarthriaMr. Alfadhel isAdvanced. Learn about Dysarthria.
- Epilepsy in ChildrenMr. Alfadhel isAdvanced. Learn about Epilepsy in Children.
- Holocarboxylase Synthetase DeficiencyMr. Alfadhel isAdvanced. Learn about Holocarboxylase Synthetase Deficiency.
- Homocystinuria due to MTHFR Deficiency
- Inborn Renal AminoaciduriaMr. Alfadhel isAdvanced. Learn about Inborn Renal Aminoaciduria.
- Infantile-Onset Spinocerebellar Ataxia (IOSCA)
- Isovaleric AcidemiaMr. Alfadhel isAdvanced. Learn about Isovaleric Acidemia.
- Lactic AcidosisMr. Alfadhel isAdvanced. Learn about Lactic Acidosis.
- Metachromatic LeukodystrophyMr. Alfadhel isAdvanced. Learn about Metachromatic Leukodystrophy.
- Methylmalonic AcidemiaMr. Alfadhel isAdvanced. Learn about Methylmalonic Acidemia.
- Microcephaly Deafness SyndromeMr. Alfadhel isAdvanced. Learn about Microcephaly Deafness Syndrome.
- Multiple Carboxylase DeficiencyMr. Alfadhel isAdvanced. Learn about Multiple Carboxylase Deficiency.
- Multiple Sulfatase DeficiencyMr. Alfadhel isAdvanced. Learn about Multiple Sulfatase Deficiency.
- Optic Nerve AtrophyMr. Alfadhel isAdvanced. Learn about Optic Nerve Atrophy.
- SpasticityMr. Alfadhel isAdvanced. Learn about Spasticity.
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Wolman DiseaseMr. Alfadhel isAdvanced. Learn about Wolman Disease.
- Experienced
- Absence SeizureMr. Alfadhel isExperienced. Learn about Absence Seizure.
- Acanthosis NigricansMr. Alfadhel isExperienced. Learn about Acanthosis Nigricans.
- Acromicric DysplasiaMr. Alfadhel isExperienced. Learn about Acromicric Dysplasia.
- Addison's DiseaseMr. Alfadhel isExperienced. Learn about Addison's Disease.
- Adrenoleukodystrophy (ALD)Mr. Alfadhel isExperienced. Learn about Adrenoleukodystrophy (ALD).
- Aicardi-Goutieres SyndromeMr. Alfadhel isExperienced. Learn about Aicardi-Goutieres Syndrome.
- AlbinismMr. Alfadhel isExperienced. Learn about Albinism.
- Angelman SyndromeMr. Alfadhel isExperienced. Learn about Angelman Syndrome.
- AnhidrosisMr. Alfadhel isExperienced. Learn about Anhidrosis.
- Aplasia Cutis CongenitaMr. Alfadhel isExperienced. Learn about Aplasia Cutis Congenita.
- ApraxiaMr. Alfadhel isExperienced. Learn about Apraxia.
- Arthrogryposis Multiplex CongenitaMr. Alfadhel isExperienced. Learn about Arthrogryposis Multiplex Congenita.
- Autonomic NeuropathyMr. Alfadhel isExperienced. Learn about Autonomic Neuropathy.
- Batten DiseaseMr. Alfadhel isExperienced. Learn about Batten Disease.
- Biotinidase DeficiencyMr. Alfadhel isExperienced. Learn about Biotinidase Deficiency.
- Brown SyndromeMr. Alfadhel isExperienced. Learn about Brown Syndrome.
- BullaeMr. Alfadhel isExperienced. Learn about Bullae.
- CalcinosisMr. Alfadhel isExperienced. Learn about Calcinosis.
- CardiomyopathyMr. Alfadhel isExperienced. Learn about Cardiomyopathy.
- CataractMr. Alfadhel isExperienced. Learn about Cataract.
- CholestasisMr. Alfadhel isExperienced. Learn about Cholestasis.
- ChoreaMr. Alfadhel isExperienced. Learn about Chorea.
- Chromosome 13q DuplicationMr. Alfadhel isExperienced. Learn about Chromosome 13q Duplication.
- Chronic Kidney DiseaseMr. Alfadhel isExperienced. Learn about Chronic Kidney Disease.
- Classic GalactosemiaMr. Alfadhel isExperienced. Learn about Classic Galactosemia.
- Cleidocranial DysplasiaMr. Alfadhel isExperienced. Learn about Cleidocranial Dysplasia.
- CLN1 DiseaseMr. Alfadhel isExperienced. Learn about CLN1 Disease.
- CLN2 DiseaseMr. Alfadhel isExperienced. Learn about CLN2 Disease.
- CLN3 DiseaseMr. Alfadhel isExperienced. Learn about CLN3 Disease.
- CLN4 DiseaseMr. Alfadhel isExperienced. Learn about CLN4 Disease.
- CLN5 DiseaseMr. Alfadhel isExperienced. Learn about CLN5 Disease.
- Clouston SyndromeMr. Alfadhel isExperienced. Learn about Clouston Syndrome.
- ClubfootMr. Alfadhel isExperienced. Learn about Clubfoot.
- Color BlindnessMr. Alfadhel isExperienced. Learn about Color Blindness.
- Cone DystrophyMr. Alfadhel isExperienced. Learn about Cone Dystrophy.
- Congenital CataractMr. Alfadhel isExperienced. Learn about Congenital Cataract.
- Congenital ContracturesMr. Alfadhel isExperienced. Learn about Congenital Contractures.
- Corpus Callosum AgenesisMr. Alfadhel isExperienced. Learn about Corpus Callosum Agenesis.
- Cranioectodermal DysplasiaMr. Alfadhel isExperienced. Learn about Cranioectodermal Dysplasia.
- CystinosisMr. Alfadhel isExperienced. Learn about Cystinosis.
- Delayed GrowthMr. Alfadhel isExperienced. Learn about Delayed Growth.
- Diabetes Insipidus (DI)Mr. Alfadhel isExperienced. Learn about Diabetes Insipidus (DI).
- Dihydrolipoamide Dehydrogenase DeficiencyMr. Alfadhel isExperienced. Learn about Dihydrolipoamide Dehydrogenase Deficiency.
- Distal ArthrogryposisMr. Alfadhel isExperienced. Learn about Distal Arthrogryposis.
- Distal Arthrogryposis Type 6Mr. Alfadhel isExperienced. Learn about Distal Arthrogryposis Type 6.
- Ectodermal DysplasiasMr. Alfadhel isExperienced. Learn about Ectodermal Dysplasias.
- EncephaloceleMr. Alfadhel isExperienced. Learn about Encephalocele.
- EpilepsyMr. Alfadhel isExperienced. Learn about Epilepsy.
- Erectile Dysfunction (ED)Mr. Alfadhel isExperienced. Learn about Erectile Dysfunction (ED).
- Fabry DiseaseMr. Alfadhel isExperienced. Learn about Fabry Disease.
- Familial Glucocorticoid DeficiencyMr. Alfadhel isExperienced. Learn about Familial Glucocorticoid Deficiency.
- Familial HypertriglyceridemiaMr. Alfadhel isExperienced. Learn about Familial Hypertriglyceridemia.
- Fructose-1,6-Bisphosphatase DeficiencyMr. Alfadhel isExperienced. Learn about Fructose-1,6-Bisphosphatase Deficiency.
- Galactokinase DeficiencyMr. Alfadhel isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMr. Alfadhel isExperienced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMr. Alfadhel isExperienced. Learn about Galactosemia.
- Galloway-Mowat SyndromeMr. Alfadhel isExperienced. Learn about Galloway-Mowat Syndrome.
- Gaucher DiseaseMr. Alfadhel isExperienced. Learn about Gaucher Disease.
- Generalized Tonic-Clonic SeizureMr. Alfadhel isExperienced. Learn about Generalized Tonic-Clonic Seizure.
- GigantismMr. Alfadhel isExperienced. Learn about Gigantism.
- Hajdu-Cheney SyndromeMr. Alfadhel isExperienced. Learn about Hajdu-Cheney Syndrome.
- Harding AtaxiaMr. Alfadhel isExperienced. Learn about Harding Ataxia.
- HemochromatosisMr. Alfadhel isExperienced. Learn about Hemochromatosis.
- Hepatorenal SyndromeMr. Alfadhel isExperienced. Learn about Hepatorenal Syndrome.
- Hereditary AtaxiaMr. Alfadhel isExperienced. Learn about Hereditary Ataxia.
- Hereditary HyperekplexiaMr. Alfadhel isExperienced. Learn about Hereditary Hyperekplexia.
- Hereditary Sensory and Autonomic Neuropathy Type 2
- Hereditary Sensory Neuropathy Type 1 (HSN1)Mr. Alfadhel isExperienced. Learn about Hereditary Sensory Neuropathy Type 1 (HSN1).
- HerniaMr. Alfadhel isExperienced. Learn about Hernia.
- Heterotaxy SyndromeMr. Alfadhel isExperienced. Learn about Heterotaxy Syndrome.
- Hiatal HerniaMr. Alfadhel isExperienced. Learn about Hiatal Hernia.
- High Blood Pressure in InfantsMr. Alfadhel isExperienced. Learn about High Blood Pressure in Infants.
- High CholesterolMr. Alfadhel isExperienced. Learn about High Cholesterol.
- HomocystinuriaMr. Alfadhel isExperienced. Learn about Homocystinuria.
- Homozygous Familial Hypercholesterolemia (HoFH)
- HydrocephalusMr. Alfadhel isExperienced. Learn about Hydrocephalus.
- HypermethioninemiaMr. Alfadhel isExperienced. Learn about Hypermethioninemia.
- Hypomelanotic DisorderMr. Alfadhel isExperienced. Learn about Hypomelanotic Disorder.
- HypothyroidismMr. Alfadhel isExperienced. Learn about Hypothyroidism.
- Inborn Amino Acid Metabolism DisorderMr. Alfadhel isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- Incontinentia PigmentiMr. Alfadhel isExperienced. Learn about Incontinentia Pigmenti.
- Krabbe DiseaseMr. Alfadhel isExperienced. Learn about Krabbe Disease.
- Leigh SyndromeMr. Alfadhel isExperienced. Learn about Leigh Syndrome.
- LeukodystrophyMr. Alfadhel isExperienced. Learn about Leukodystrophy.
- Limb-Girdle Muscular DystrophyMr. Alfadhel isExperienced. Learn about Limb-Girdle Muscular Dystrophy.
- Livedo ReticularisMr. Alfadhel isExperienced. Learn about Livedo Reticularis.
- Liver FailureMr. Alfadhel isExperienced. Learn about Liver Failure.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Low Blood SugarMr. Alfadhel isExperienced. Learn about Low Blood Sugar.
- Lysinuric Protein IntoleranceMr. Alfadhel isExperienced. Learn about Lysinuric Protein Intolerance.
- Lysosomal Acid Lipase DeficiencyMr. Alfadhel isExperienced. Learn about Lysosomal Acid Lipase Deficiency.
- MalabsorptionMr. Alfadhel isExperienced. Learn about Malabsorption.
- MalnutritionMr. Alfadhel isExperienced. Learn about Malnutrition.
- Meckel SyndromeMr. Alfadhel isExperienced. Learn about Meckel Syndrome.
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- MELAS SyndromeMr. Alfadhel isExperienced. Learn about MELAS Syndrome.
- MelasmaMr. Alfadhel isExperienced. Learn about Melasma.
- Metabolic AcidosisMr. Alfadhel isExperienced. Learn about Metabolic Acidosis.
- MicrognathiaMr. Alfadhel isExperienced. Learn about Micrognathia.
- Microvillus Inclusion DiseaseMr. Alfadhel isExperienced. Learn about Microvillus Inclusion Disease.
- Mitochondrial Complex 1 DeficiencyMr. Alfadhel isExperienced. Learn about Mitochondrial Complex 1 Deficiency.
- Movement DisordersMr. Alfadhel isExperienced. Learn about Movement Disorders.
- Mucolipidosis 3Mr. Alfadhel isExperienced. Learn about Mucolipidosis 3.
- Mucolipidosis Type 4Mr. Alfadhel isExperienced. Learn about Mucolipidosis Type 4.
- N-Acetylglutamate Synthase DeficiencyMr. Alfadhel isExperienced. Learn about N-Acetylglutamate Synthase Deficiency.
- NephrocalcinosisMr. Alfadhel isExperienced. Learn about Nephrocalcinosis.
- Niemann-Pick DiseaseMr. Alfadhel isExperienced. Learn about Niemann-Pick Disease.
- ObesityMr. Alfadhel isExperienced. Learn about Obesity.
- Olivopontocerebellar AtrophyMr. Alfadhel isExperienced. Learn about Olivopontocerebellar Atrophy.
- ParaplegiaMr. Alfadhel isExperienced. Learn about Paraplegia.
- Pelizaeus-Merzbacher DiseaseMr. Alfadhel isExperienced. Learn about Pelizaeus-Merzbacher Disease.
- Phenylketonuria (PKU)Mr. Alfadhel isExperienced. Learn about Phenylketonuria (PKU).
- PMM2-Congenital Disorder of GlycosylationMr. Alfadhel isExperienced. Learn about PMM2-Congenital Disorder of Glycosylation.
- Primary Carnitine DeficiencyMr. Alfadhel isExperienced. Learn about Primary Carnitine Deficiency.
- Primary HyperoxaluriaMr. Alfadhel isExperienced. Learn about Primary Hyperoxaluria.
- Pyruvate Decarboxylase DeficiencyMr. Alfadhel isExperienced. Learn about Pyruvate Decarboxylase Deficiency.
- Pyruvate Dehydrogenase DeficiencyMr. Alfadhel isExperienced. Learn about Pyruvate Dehydrogenase Deficiency.
- Restrictive Cardiomyopathy (RCM)Mr. Alfadhel isExperienced. Learn about Restrictive Cardiomyopathy (RCM).
- Riboflavin Transporter Deficiency Neuronopathy
- ScoliosisMr. Alfadhel isExperienced. Learn about Scoliosis.
- SeizuresMr. Alfadhel isExperienced. Learn about Seizures.
- Short Stature (Growth Disorders)Mr. Alfadhel isExperienced. Learn about Short Stature (Growth Disorders).
- SialidosisMr. Alfadhel isExperienced. Learn about Sialidosis.
- Spasmus NutansMr. Alfadhel isExperienced. Learn about Spasmus Nutans.
- Spastic Paraplegia Type 2Mr. Alfadhel isExperienced. Learn about Spastic Paraplegia Type 2.
- Spastic Paraplegia Type 7Mr. Alfadhel isExperienced. Learn about Spastic Paraplegia Type 7.
- Spinocerebellar AtaxiaMr. Alfadhel isExperienced. Learn about Spinocerebellar Ataxia.
- Spinocerebellar Ataxia Type 8Mr. Alfadhel isExperienced. Learn about Spinocerebellar Ataxia Type 8.
- Stiff Person SyndromeMr. Alfadhel isExperienced. Learn about Stiff Person Syndrome.
- SyndactylyMr. Alfadhel isExperienced. Learn about Syndactyly.
- Transcobalamin DeficiencyMr. Alfadhel isExperienced. Learn about Transcobalamin Deficiency.
- TrimethylaminuriaMr. Alfadhel isExperienced. Learn about Trimethylaminuria.
- Trisomy 13Mr. Alfadhel isExperienced. Learn about Trisomy 13.
- Trisomy 18Mr. Alfadhel isExperienced. Learn about Trisomy 18.
- Umbilical HerniaMr. Alfadhel isExperienced. Learn about Umbilical Hernia.
- Undescended TesticleMr. Alfadhel isExperienced. Learn about Undescended Testicle.
- Urea Cycle Disorders (UCD)Mr. Alfadhel isExperienced. Learn about Urea Cycle Disorders (UCD).
- West SyndromeMr. Alfadhel isExperienced. Learn about West Syndrome.
- Zellweger SyndromeMr. Alfadhel isExperienced. Learn about Zellweger Syndrome.