Overview
Hans Andersson is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Metairie, Louisiana.
Dr. Andersson is highly rated in 10 conditions, according to our data. His clinical expertise encompasses Phenylketonuria (PKU), Gaucher Disease Type 1, Inborn Amino Acid Metabolism Disorder, Maternal Hyperphenylalaninemia, and Splenectomy.
He is actively involved in clinical research, co-authoring 36 peer reviewed articles and participating in 1 clinical trial. Dr. Andersson is currently accepting new patients.
Specialties
Licenses
Hospital Affiliations
Languages Spoken
Gender
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- HMO
- MANAGED MEDICAID PLAN
- OTHER MEDICAID
- STATE MEDICAID
- EPO
- HMO
- POS
- PPO
Locations
3040 33rd St, Metairie, LA 70001
220 W Willow St Bldg A, Lafayette Public Health Unit, Lafayette, LA 70501
1029 Capitol Ave, Crowley, LA 70526
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers 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.
1 Clinical Trials
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Louisiana State University School Of Medicine In New Orleans Faculty G
Sun Kim is a Medical Genetics specialist and a Pediatrics provider practicing medicine in New Orleans, Louisiana. Dr. Kim is highly rated in 37 conditions, according to our data. Her clinical expertise encompasses Chromosome 13q Deletion, Neurofibromatosis Type 1 (NF1), Neurofibromatosis, and Cat Eye Syndrome.
Yves Lacassie is a Medical Genetics specialist and a Pediatrics provider practicing medicine in New Orleans, Louisiana. Dr. Lacassie is highly rated in 5 conditions, according to our data. His clinical expertise encompasses Crouzon Syndrome, Learman Syndrome, Ring Chromosome 13, and Multiple Synostoses Syndrome 1.
Frequently Asked Questions about Dr. Hans C. Andersson
How do I make an appointment with Dr. Hans C. Andersson?
You can book an appointment with Dr. Hans C. Andersson by calling their office at 504-219-0880. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Hans C. Andersson a top-rated expert for Phenylketonuria (PKU)?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Hans C. Andersson is classified as an Distinguished expert for Phenylketonuria (PKU), 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.
What conditions does Dr. Hans C. Andersson specialize in?
While Dr. Hans C. Andersson is a Medical Genetics, they have specific expertise in Phenylketonuria (PKU), Gaucher Disease Type 1, and Inborn Amino Acid Metabolism Disorder. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Hans C. Andersson participate in research or clinical trials?
Yes. Dr. Hans C. Andersson has published 36 articles and abstracts on conditions like Phenylketonuria (PKU). You can view a list of Dr. Hans C. Andersson's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Hans C. Andersson accept my insurance?
Dr. Hans C. Andersson accepts most major insurance plans, including Aetna and Blue Cross Blue Shield. We recommend calling the office directly at 504-219-0880 to verify that your specific plan is currently accepted before your visit.
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
- Phenylketonuria (PKU)Dr. Andersson isDistinguished. Learn about Phenylketonuria (PKU).
- Advanced
- Classic GalactosemiaDr. Andersson isAdvanced. Learn about Classic Galactosemia.
- Gaucher Disease Type 1Dr. Andersson isAdvanced. Learn about Gaucher Disease Type 1.
- Inborn Amino Acid Metabolism DisorderDr. Andersson isAdvanced. Learn about Inborn Amino Acid Metabolism Disorder.
- Maple Syrup Urine DiseaseDr. Andersson isAdvanced. Learn about Maple Syrup Urine Disease.
- Maternal HyperphenylalaninemiaDr. Andersson isAdvanced. Learn about Maternal Hyperphenylalaninemia.
- Methylmalonic AcidemiaDr. Andersson isAdvanced. Learn about Methylmalonic Acidemia.
- Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)
- Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome)
- Propionic AcidemiaDr. Andersson isAdvanced. Learn about Propionic Acidemia.
- Experienced
- 15q11.2 MicrodeletionDr. Andersson isExperienced. Learn about 15q11.2 Microdeletion.
- 3p Deletion SyndromeDr. Andersson isExperienced. Learn about 3p Deletion Syndrome.
- Autism Spectrum DisorderDr. Andersson isExperienced. Learn about Autism Spectrum Disorder.
- Biotinidase DeficiencyDr. Andersson isExperienced. Learn about Biotinidase Deficiency.
- BrachydactylyDr. Andersson isExperienced. Learn about Brachydactyly.
- Cardiofaciocutaneous SyndromeDr. Andersson isExperienced. Learn about Cardiofaciocutaneous Syndrome.
- Cardiomyopathic LentiginosisDr. Andersson isExperienced. Learn about Cardiomyopathic Lentiginosis.
- Chromosome 12p DeletionDr. Andersson isExperienced. Learn about Chromosome 12p Deletion.
- Chromosome 15q DeletionDr. Andersson isExperienced. Learn about Chromosome 15q Deletion.
- Chromosome 18p DeletionDr. Andersson isExperienced. Learn about Chromosome 18p Deletion.
- Chromosome 21q DeletionDr. Andersson isExperienced. Learn about Chromosome 21q Deletion.
- Chromosome 4q DeletionDr. Andersson isExperienced. Learn about Chromosome 4q Deletion.
- Chromosome 6q DeletionDr. Andersson isExperienced. Learn about Chromosome 6q Deletion.
- Chromosome 6q DuplicationDr. Andersson isExperienced. Learn about Chromosome 6q Duplication.
- Chromosome 7p DeletionDr. Andersson isExperienced. Learn about Chromosome 7p Deletion.
- Chromosome 8p DeletionDr. Andersson isExperienced. Learn about Chromosome 8p Deletion.
- Chromosome 9p DeletionDr. Andersson isExperienced. Learn about Chromosome 9p Deletion.
- CitrullinemiaDr. Andersson isExperienced. Learn about Citrullinemia.
- Dihydropteridine Reductase DeficiencyDr. Andersson isExperienced. Learn about Dihydropteridine Reductase Deficiency.
- Distal 18q Deletion SyndromeDr. Andersson isExperienced. Learn about Distal 18q Deletion Syndrome.
- Fabry DiseaseDr. Andersson isExperienced. Learn about Fabry Disease.
- Farber LipogranulomatosisDr. Andersson isExperienced. Learn about Farber Lipogranulomatosis.
- Galactokinase DeficiencyDr. Andersson isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyDr. Andersson isExperienced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaDr. Andersson isExperienced. Learn about Galactosemia.
- Gaucher DiseaseDr. Andersson isExperienced. Learn about Gaucher Disease.
- Gaucher Disease Type 2Dr. Andersson isExperienced. Learn about Gaucher Disease Type 2.
- Gaucher Disease Type 3Dr. Andersson isExperienced. Learn about Gaucher Disease Type 3.
- IntersexDr. Andersson isExperienced. Learn about Intersex.
- Isovaleric AcidemiaDr. Andersson isExperienced. Learn about Isovaleric Acidemia.
- Jacobsen SyndromeDr. Andersson isExperienced. Learn about Jacobsen Syndrome.
- Leigh SyndromeDr. Andersson isExperienced. Learn about Leigh Syndrome.
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Megalencephalic Leukoencephalopathy with Subcortical Cysts
- Mucopolysaccharidoses (MPS)Dr. Andersson isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Multiple Sulfatase DeficiencyDr. Andersson isExperienced. Learn about Multiple Sulfatase Deficiency.
- N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3
- NeurofibromatosisDr. Andersson isExperienced. Learn about Neurofibromatosis.
- Neurofibromatosis Type 1 (NF1)Dr. Andersson isExperienced. Learn about Neurofibromatosis Type 1 (NF1).
- Niemann-Pick DiseaseDr. Andersson isExperienced. Learn about Niemann-Pick Disease.
- Noonan SyndromeDr. Andersson isExperienced. Learn about Noonan Syndrome.
- Ornithine Transcarbamylase DeficiencyDr. Andersson isExperienced. Learn about Ornithine Transcarbamylase Deficiency.
- Ornithine Translocase DeficiencyDr. Andersson isExperienced. Learn about Ornithine Translocase Deficiency.
- RASopathiesDr. Andersson isExperienced. Learn about RASopathies.
- Short Stature (Growth Disorders)Dr. Andersson isExperienced. Learn about Short Stature (Growth Disorders).
- SplenectomyDr. Andersson isExperienced. Learn about Splenectomy.
- Turner SyndromeDr. Andersson isExperienced. Learn about Turner Syndrome.
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Y Chromosome InfertilityDr. Andersson isExperienced. Learn about Y Chromosome Infertility.
- Zellweger SyndromeDr. Andersson isExperienced. Learn about Zellweger Syndrome.