Overview
Ahmad Alahmad practices practicing medicine in Kuwait City, Kuwait.
Mr. Alahmad is highly rated in 3 conditions, according to our data. His clinical expertise encompasses Mitochondrial Complex 3 Deficiency, Coenzyme Q Cytochrome C Reductase Deficiency, Leigh Syndrome, and Fountain Syndrome.
He is actively involved in clinical research, co-authoring 17 peer reviewed articles.
Gender
Locations
Ministry Of Health, Kuwait
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 Ahmad M. Alahmad
Is Ahmad M. Alahmad a top-rated expert for Mitochondrial Complex 3 Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Ahmad M. Alahmad is classified as an Distinguished expert for Mitochondrial Complex 3 Deficiency, 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 Ahmad M. Alahmad participate in research or clinical trials?
Yes. Ahmad M. Alahmad has published 17 articles and abstracts on conditions like Mitochondrial Complex 3 Deficiency. You can view a list of Ahmad M. Alahmad'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
- Coenzyme Q Cytochrome C Reductase DeficiencyMr. Alahmad isDistinguished. Learn about Coenzyme Q Cytochrome C Reductase Deficiency.
- Mitochondrial Complex 3 DeficiencyMr. Alahmad isDistinguished. Learn about Mitochondrial Complex 3 Deficiency.
- Advanced
- Leigh SyndromeMr. Alahmad isAdvanced. Learn about Leigh Syndrome.
- Experienced
- AnhidrosisMr. Alahmad isExperienced. Learn about Anhidrosis.
- ChoreaMr. Alahmad isExperienced. Learn about Chorea.
- Congenital CataractMr. Alahmad isExperienced. Learn about Congenital Cataract.
- Drug Induced DyskinesiaMr. Alahmad isExperienced. Learn about Drug Induced Dyskinesia.
- DysarthriaMr. Alahmad isExperienced. Learn about Dysarthria.
- Fountain SyndromeMr. Alahmad isExperienced. Learn about Fountain Syndrome.
- Hajdu-Cheney SyndromeMr. Alahmad isExperienced. Learn about Hajdu-Cheney Syndrome.
- Hereditary Sensory and Autonomic Neuropathy Type 2
- Hereditary Sensory Neuropathy Type 1 (HSN1)
- HomocystinuriaMr. Alahmad isExperienced. Learn about Homocystinuria.
- HypotoniaMr. Alahmad isExperienced. Learn about Hypotonia.
- Lactic AcidosisMr. Alahmad isExperienced. Learn about Lactic Acidosis.
- Mitochondrial Complex 1 DeficiencyMr. Alahmad isExperienced. Learn about Mitochondrial Complex 1 Deficiency.
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency