Overview
Madelena Martin is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Sacramento, California.
Dr. Martin is highly rated in 12 conditions, according to our data. Her clinical expertise encompasses Danon Disease, Pompe Disease, Phenylketonuria (PKU), and Fabry Disease.
Dr. Martin is board certified in Medical Genetics And Genomics Clin Genetics & Genomic and Medical Genetics And Genomics Clin Biochemical Genetic. She is actively involved in clinical research, co-authoring 5 peer reviewed articles and participating in 1 clinical trial. Dr. Martin is currently accepting new patients.
Graduate Institution
Specialties
Licenses
Board Certifications
Fellowships
Hospital Affiliations
Languages Spoken
Gender
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE-MEDICAID PLAN
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- EPO
- HMO
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
Accepted plan types not found. Please verify directly with the provider.
- HMO
- INDEMNITY
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- HMO
- OTHER COMMERCIAL
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
- HMO
- INSURANCE PLAN
- MEDICARE DISCOUNT CARD
- MEDICARE MAPD
Locations
2825 50th St, Sacramento, CA 95817
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
Katherine Rauen is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Sacramento, California. Dr. Rauen is highly rated in 9 conditions, according to our data. Her clinical expertise encompasses RASopathies, Costello Syndrome, Legius Syndrome, and Cardiofaciocutaneous Syndrome.
UC Davis Medical Center MIND Institute
Suma Shankar is a Medical Genetics provider practicing medicine in Sacramento, California. Dr. Shankar is highly rated in 16 conditions, according to our data. Her clinical expertise encompasses Gaucher Disease Type 1, RASopathies, Costello Syndrome, and Fabry Disease. Dr. Shankar is board certified in Medical Genetics And Genomics Clin Genetics & Genomic. Dr. Shankar is currently accepting new patients.
UC Davis Medical Center MIND Institute
Kristin Herman is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Sacramento, California. Dr. Herman is highly rated in 33 conditions, according to our data. Her clinical expertise encompasses Brittle Cornea Syndrome, Vascular Ehlers-Danlos Syndrome (VEDS), Musculocontractural Ehlers-Danlos Syndrome (mcEDS), and Hypotonia. Dr. Herman is board certified in Medical Genetics And Genomics Clin Genetics & Genomic and Pediatrics. Dr. Herman is currently accepting new patients.
Frequently Asked Questions about Dr. Madelena M. Martin
How do I make an appointment with Dr. Madelena M. Martin?
You can book an appointment with Dr. Madelena M. Martin by calling their office at 916-703-0235. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Madelena M. Martin a top-rated expert for Danon Disease?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Madelena M. Martin is classified as an Distinguished expert for Danon Disease, 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. Madelena M. Martin specialize in?
While Dr. Madelena M. Martin is a Medical Genetics, they have specific expertise in Danon Disease, Pompe Disease, and Phenylketonuria (PKU). MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Madelena M. Martin participate in research or clinical trials?
Yes. Dr. Madelena M. Martin has published 5 articles and abstracts on conditions like Danon Disease. You can view a list of Dr. Madelena M. Martin's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Madelena M. Martin accept my insurance?
Dr. Madelena M. Martin accepts most major insurance plans, including Anthem BCBS and Blue Shield of California. We recommend calling the office directly at 916-703-0235 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
- Danon DiseaseDr. Martin isDistinguished. Learn about Danon Disease.
- Pompe DiseaseDr. Martin isDistinguished. Learn about Pompe Disease.
- Advanced
- Dihydropteridine Reductase Deficiency
- Fabry DiseaseDr. Martin isAdvanced. Learn about Fabry Disease.
- Maternal HyperphenylalaninemiaDr. Martin isAdvanced. Learn about Maternal Hyperphenylalaninemia.
- Megalencephalic Leukoencephalopathy with Subcortical Cysts
- MELAS SyndromeDr. Martin isAdvanced. Learn about MELAS Syndrome.
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Multiple Sulfatase DeficiencyDr. Martin isAdvanced. Learn about Multiple Sulfatase Deficiency.
- Ornithine Transcarbamylase Deficiency
- Ornithine Translocase DeficiencyDr. Martin isAdvanced. Learn about Ornithine Translocase Deficiency.
- Phenylketonuria (PKU)Dr. Martin isAdvanced. Learn about Phenylketonuria (PKU).
- Experienced
- AcrocephalopolydactylyDr. Martin isExperienced. Learn about Acrocephalopolydactyly.
- Acromegaloid Facial Appearance SyndromeDr. Martin isExperienced. Learn about Acromegaloid Facial Appearance Syndrome.
- Apert SyndromeDr. Martin isExperienced. Learn about Apert Syndrome.
- Autosomal Cleft PalateDr. Martin isExperienced. Learn about Autosomal Cleft Palate.
- Cholesteryl Ester Storage DiseaseDr. Martin isExperienced. Learn about Cholesteryl Ester Storage Disease.
- Chromosome 11 Uniparental DisomyDr. Martin isExperienced. Learn about Chromosome 11 Uniparental Disomy.
- Chromosome 2 Uniparental DisomyDr. Martin isExperienced. Learn about Chromosome 2 Uniparental Disomy.
- Chromosome 6 Uniparental DisomyDr. Martin isExperienced. Learn about Chromosome 6 Uniparental Disomy.
- Classic GalactosemiaDr. Martin isExperienced. Learn about Classic Galactosemia.
- Cleft Lip and PalateDr. Martin isExperienced. Learn about Cleft Lip and Palate.
- Deafness Craniofacial SyndromeDr. Martin isExperienced. Learn about Deafness Craniofacial Syndrome.
- Fraser SyndromeDr. Martin isExperienced. Learn about Fraser Syndrome.
- Galactose Epimerase DeficiencyDr. Martin isExperienced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaDr. Martin isExperienced. Learn about Galactosemia.
- Gaucher DiseaseDr. Martin isExperienced. Learn about Gaucher Disease.
- Gaucher Disease Type 1Dr. Martin isExperienced. Learn about Gaucher Disease Type 1.
- Gaucher Disease Type 2Dr. Martin isExperienced. Learn about Gaucher Disease Type 2.
- Gaucher Disease Type 3Dr. Martin isExperienced. Learn about Gaucher Disease Type 3.
- Glycogen Storage Disease Type 3Dr. Martin isExperienced. Learn about Glycogen Storage Disease Type 3.
- Hereditary CoproporphyriaDr. Martin isExperienced. Learn about Hereditary Coproporphyria.
- Hereditary Sensory and Autonomic Neuropathy Type 2
- Hereditary Sensory Neuropathy Type 1 (HSN1)
- Hereditary XanthinuriaDr. Martin isExperienced. Learn about Hereditary Xanthinuria.
- Hypertrichosis-Acromegaloid Facial Appearance Syndrome
- Inborn Amino Acid Metabolism DisorderDr. Martin isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- Lysosomal Acid Lipase DeficiencyDr. Martin isExperienced. Learn about Lysosomal Acid Lipase Deficiency.
- Menkes DiseaseDr. Martin isExperienced. Learn about Menkes Disease.
- Methylmalonic AcidemiaDr. Martin isExperienced. Learn about Methylmalonic Acidemia.
- MicrognathiaDr. Martin isExperienced. Learn about Micrognathia.
- Mosaic Variegated Aneuploidy SyndromeDr. Martin isExperienced. Learn about Mosaic Variegated Aneuploidy Syndrome.
- Mucopolysaccharidoses (MPS)Dr. Martin isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Multiple Epiphyseal DysplasiaDr. Martin isExperienced. Learn about Multiple Epiphyseal Dysplasia.
- Oral-Facial-Digital SyndromeDr. Martin isExperienced. Learn about Oral-Facial-Digital Syndrome.
- Orotic Aciduria Type 1Dr. Martin isExperienced. Learn about Orotic Aciduria Type 1.
- Otopalatodigital Syndrome Type 1Dr. Martin isExperienced. Learn about Otopalatodigital Syndrome Type 1.
- Pallister-Killian Mosaic SyndromeDr. Martin isExperienced. Learn about Pallister-Killian Mosaic Syndrome.
- Pfeiffer SyndromeDr. Martin isExperienced. Learn about Pfeiffer Syndrome.
- Pierre Robin SequenceDr. Martin isExperienced. Learn about Pierre Robin Sequence.
- Propionic AcidemiaDr. Martin isExperienced. Learn about Propionic Acidemia.
- Saethre-Chotzen SyndromeDr. Martin isExperienced. Learn about Saethre-Chotzen Syndrome.
- Temple SyndromeDr. Martin isExperienced. Learn about Temple Syndrome.
- Tetrasomy 9pDr. Martin isExperienced. Learn about Tetrasomy 9p.
- Thymidine Kinase 2 Deficiency (TK2d)Dr. Martin isExperienced. Learn about Thymidine Kinase 2 Deficiency (TK2d).
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Wolman DiseaseDr. Martin isExperienced. Learn about Wolman Disease.