Overview
David Coman practices practicing medicine in South Brisbane, Australia.
Mr. Coman is highly rated in 15 conditions, according to our data. His clinical expertise encompasses Ataxia-Telangiectasia, Classic Galactosemia, Telangiectasia, and Galactokinase Deficiency.
He is actively involved in clinical research, co-authoring 94 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 David J. Coman
Is David J. Coman a top-rated expert for Ataxia-Telangiectasia?
MediFind is an objective health platform that identifies experts based on real-world data. David J. Coman is classified as an Distinguished expert for Ataxia-Telangiectasia, 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 David J. Coman participate in research or clinical trials?
Yes. David J. Coman has published 94 articles and abstracts on conditions like Ataxia-Telangiectasia. You can view a list of David J. Coman'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
- Ataxia-TelangiectasiaMr. Coman isDistinguished. Learn about Ataxia-Telangiectasia.
- Classic GalactosemiaMr. Coman isDistinguished. Learn about Classic Galactosemia.
- Advanced
- Bone Dysplasia Corpus Callosum Agenesis
- Carnitine-Acylcarnitine Translocase Deficiency
- Familial Wilms Tumor 2Mr. Coman isAdvanced. Learn about Familial Wilms Tumor 2.
- Galactokinase DeficiencyMr. Coman isAdvanced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMr. Coman isAdvanced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMr. Coman isAdvanced. Learn about Galactosemia.
- Holocarboxylase Synthetase Deficiency
- Lactic AcidosisMr. Coman isAdvanced. Learn about Lactic Acidosis.
- MicrognathiaMr. Coman isAdvanced. Learn about Micrognathia.
- Orotic Aciduria Type 1Mr. Coman isAdvanced. Learn about Orotic Aciduria Type 1.
- Pontocerebellar HypoplasiaMr. Coman isAdvanced. Learn about Pontocerebellar Hypoplasia.
- SpondyloenchondrodysplasiaMr. Coman isAdvanced. Learn about Spondyloenchondrodysplasia.
- TelangiectasiaMr. Coman isAdvanced. Learn about Telangiectasia.
- Experienced
- ApraxiaMr. Coman isExperienced. Learn about Apraxia.
- Arthrogryposis Multiplex CongenitaMr. Coman isExperienced. Learn about Arthrogryposis Multiplex Congenita.
- Brachydactyly Mononen TypeMr. Coman isExperienced. Learn about Brachydactyly Mononen Type.
- CardiomyopathyMr. Coman isExperienced. Learn about Cardiomyopathy.
- CataractMr. Coman isExperienced. Learn about Cataract.
- Cerebellar HypoplasiaMr. Coman isExperienced. Learn about Cerebellar Hypoplasia.
- ChondrodystrophyMr. Coman isExperienced. Learn about Chondrodystrophy.
- Coffin-Siris SyndromeMr. Coman isExperienced. Learn about Coffin-Siris Syndrome.
- Congenital ContracturesMr. Coman isExperienced. Learn about Congenital Contractures.
- Corpus Callosum AgenesisMr. Coman isExperienced. Learn about Corpus Callosum Agenesis.
- Cortical DysplasiaMr. Coman isExperienced. Learn about Cortical Dysplasia.
- DehydrationMr. Coman isExperienced. Learn about Dehydration.
- Denys-Drash Syndrome (DDS)Mr. Coman isExperienced. Learn about Denys-Drash Syndrome (DDS).
- DiarrheaMr. Coman isExperienced. Learn about Diarrhea.
- Drug Induced DyskinesiaMr. Coman isExperienced. Learn about Drug Induced Dyskinesia.
- DysarthriaMr. Coman isExperienced. Learn about Dysarthria.
- EpilepsyMr. Coman isExperienced. Learn about Epilepsy.
- Epilepsy Juvenile AbsenceMr. Coman isExperienced. Learn about Epilepsy Juvenile Absence.
- Exocrine Pancreatic InsufficiencyMr. Coman isExperienced. Learn about Exocrine Pancreatic Insufficiency.
- Frasier SyndromeMr. Coman isExperienced. Learn about Frasier Syndrome.
- Glutaric Acidemia Type 2Mr. Coman isExperienced. Learn about Glutaric Acidemia Type 2.
- Hajdu-Cheney SyndromeMr. Coman isExperienced. Learn about Hajdu-Cheney Syndrome.
- Hallervorden-Spatz DiseaseMr. Coman isExperienced. Learn about Hallervorden-Spatz Disease.
- Hearing LossMr. Coman isExperienced. Learn about Hearing Loss.
- Hereditary Sensory and Autonomic Neuropathy Type 2
- Hypophosphatasia (HPP)Mr. Coman isExperienced. Learn about Hypophosphatasia (HPP).
- HypothyroidismMr. Coman isExperienced. Learn about Hypothyroidism.
- HypotoniaMr. Coman isExperienced. Learn about Hypotonia.
- Increased Head CircumferenceMr. Coman isExperienced. Learn about Increased Head Circumference.
- Infant Respiratory Distress SyndromeMr. Coman isExperienced. Learn about Infant Respiratory Distress Syndrome.
- L-2-Hydroxyglutaric AciduriaMr. Coman isExperienced. Learn about L-2-Hydroxyglutaric Aciduria.
- Leber Hereditary Optic Neuropathy (LHON)
- Leigh SyndromeMr. Coman isExperienced. Learn about Leigh Syndrome.
- LissencephalyMr. Coman isExperienced. Learn about Lissencephaly.
- Lissencephaly 1Mr. Coman isExperienced. Learn about Lissencephaly 1.
- Liver FailureMr. Coman isExperienced. Learn about Liver Failure.
- Low Blood SugarMr. Coman isExperienced. Learn about Low Blood Sugar.
- Maternal HyperphenylalaninemiaMr. Coman isExperienced. Learn about Maternal Hyperphenylalaninemia.
- Membranoproliferative Glomerulonephritis
- Metabolic AcidosisMr. Coman isExperienced. Learn about Metabolic Acidosis.
- Mevalonate Kinase DeficiencyMr. Coman isExperienced. Learn about Mevalonate Kinase Deficiency.
- MicrophthalmiaMr. Coman isExperienced. Learn about Microphthalmia.
- Miller SyndromeMr. Coman isExperienced. Learn about Miller Syndrome.
- Miller-Dieker SyndromeMr. Coman isExperienced. Learn about Miller-Dieker Syndrome.
- Mitochondrial Trifunctional Protein Deficiency
- Multiple Carboxylase DeficiencyMr. Coman isExperienced. Learn about Multiple Carboxylase Deficiency.
- MyelitisMr. Coman isExperienced. Learn about Myelitis.
- N-Acetylglutamate Synthase DeficiencyMr. Coman isExperienced. Learn about N-Acetylglutamate Synthase Deficiency.
- Neonatal HypothyroidismMr. Coman isExperienced. Learn about Neonatal Hypothyroidism.
- NeurosarcoidosisMr. Coman isExperienced. Learn about Neurosarcoidosis.
- PGM1-CDGMr. Coman isExperienced. Learn about PGM1-CDG.
- Phenylketonuria (PKU)Mr. Coman isExperienced. Learn about Phenylketonuria (PKU).
- PMM2-Congenital Disorder of Glycosylation
- Protein DeficiencyMr. Coman isExperienced. Learn about Protein Deficiency.
- Schwartz-Jampel SyndromeMr. Coman isExperienced. Learn about Schwartz-Jampel Syndrome.
- SeizuresMr. Coman isExperienced. Learn about Seizures.
- Short Stature (Growth Disorders)Mr. Coman isExperienced. Learn about Short Stature (Growth Disorders).
- Smith-Kingsmore SyndromeMr. Coman isExperienced. Learn about Smith-Kingsmore Syndrome.
- Smith-Lemli-Opitz SyndromeMr. Coman isExperienced. Learn about Smith-Lemli-Opitz Syndrome.
- Spastic Paraplegia Type 2Mr. Coman isExperienced. Learn about Spastic Paraplegia Type 2.
- SpasticityMr. Coman isExperienced. Learn about Spasticity.
- Spinocerebellar Ataxia Type 8Mr. Coman isExperienced. Learn about Spinocerebellar Ataxia Type 8.
- Subcortical Band HeterotopiaMr. Coman isExperienced. Learn about Subcortical Band Heterotopia.
- Transverse MyelitisMr. Coman isExperienced. Learn about Transverse Myelitis.
- Turner SyndromeMr. Coman isExperienced. Learn about Turner Syndrome.
- Urea Cycle Disorders (UCD)Mr. Coman isExperienced. Learn about Urea Cycle Disorders (UCD).
- X-Linked Spondyloepiphyseal Dysplasia Tarda