Overview
Kumarie Latchman is a Medical Genetics provider in Miami, Florida. Dr. Latchman is highly rated in 2 conditions, according to our data. Her top areas of expertise are Classic Galactosemia, Early Infantile Epileptic Encephalopathy, Choanal Atresia, and Galactose Epimerase Deficiency. Dr. Latchman is currently accepting new patients.
Her clinical research consists of co-authoring 5 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Specialties
Licenses
Languages Spoken
Gender
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- PPO
- HMO
- POS
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- EPO
- HMO
- PPO
- EPO
- HMO
- POS
- PPO
Locations
1611 Nw 12 Ave, Miami, FL 33136
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.
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Frequently Asked Questions about Dr. Kumarie Latchman
How do I make an appointment with Dr. Kumarie Latchman?
You can book an appointment with Dr. Kumarie Latchman by calling their office at 305-243-3100. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Kumarie Latchman a top-rated expert for Classic Galactosemia?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Kumarie Latchman is classified as an Advanced expert for Classic Galactosemia, 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. Kumarie Latchman specialize in?
While Dr. Kumarie Latchman is a Medical Genetics, they have specific expertise in Classic Galactosemia, Early Infantile Epileptic Encephalopathy, and Choanal Atresia. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Kumarie Latchman participate in research or clinical trials?
Yes. Dr. Kumarie Latchman has published 5 articles and abstracts on conditions like Classic Galactosemia. You can view a list of Dr. Kumarie Latchman's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Kumarie Latchman accept my insurance?
Dr. Kumarie Latchman accepts most major insurance plans, including Aetna and Florida Blue. We recommend calling the office directly at 305-243-3100 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
- Advanced
- Classic GalactosemiaDr. Latchman isAdvanced. Learn about Classic Galactosemia.
- Early Infantile Epileptic Encephalopathy
- Experienced
- Achalasia Microcephaly SyndromeDr. Latchman isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Angelman SyndromeDr. Latchman isExperienced. Learn about Angelman Syndrome.
- Choanal AtresiaDr. Latchman isExperienced. Learn about Choanal Atresia.
- Cortical DysplasiaDr. Latchman isExperienced. Learn about Cortical Dysplasia.
- Galactokinase DeficiencyDr. Latchman isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyDr. Latchman isExperienced. Learn about Galactose Epimerase Deficiency.