Overview
Mauricio De Castro Pretelt is a Medical Genetics specialist and a Pediatrics provider in Keesler Afb, Mississippi. Dr. De Castro Pretelt is highly rated in 2 conditions, according to our data. His top areas of expertise are Chondrodysplasia Punctata with Steroid Sulfatase Deficiency, Multiple Sulfatase Deficiency, Biotinidase Deficiency, and Pyruvate Carboxylase Deficiency.
His clinical research consists of co-authoring 22 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Specialties
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Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- HMO
- INDEMNITY
- POS
- PPO
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. 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. Mauricio J. De Castro Pretelt
How do I make an appointment with Dr. Mauricio J. De Castro Pretelt?
You can book an appointment with Dr. Mauricio J. De Castro Pretelt by calling their office at 228-376-3389. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Mauricio J. De Castro Pretelt a top-rated expert for Chondrodysplasia Punctata with Steroid Sulfatase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Mauricio J. De Castro Pretelt is classified as an Distinguished expert for Chondrodysplasia Punctata with Steroid Sulfatase 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.
What conditions does Dr. Mauricio J. De Castro Pretelt specialize in?
While Dr. Mauricio J. De Castro Pretelt is a Medical Genetics, they have specific expertise in Chondrodysplasia Punctata with Steroid Sulfatase Deficiency, Multiple Sulfatase Deficiency, and Biotinidase Deficiency. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Mauricio J. De Castro Pretelt participate in research or clinical trials?
Yes. Dr. Mauricio J. De Castro Pretelt has published 21 articles and abstracts on conditions like Chondrodysplasia Punctata with Steroid Sulfatase Deficiency. You can view a list of Dr. Mauricio J. De Castro Pretelt's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Mauricio J. De Castro Pretelt accept my insurance?
Dr. Mauricio J. De Castro Pretelt accepts most major insurance plans, including Humana. We recommend calling the office directly at 228-376-3389 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
- Chondrodysplasia Punctata with Steroid Sulfatase DeficiencyDr. De Castro Pretelt isDistinguished. Learn about Chondrodysplasia Punctata with Steroid Sulfatase Deficiency.
- Multiple Sulfatase DeficiencyDr. De Castro Pretelt isDistinguished. Learn about Multiple Sulfatase Deficiency.
- Experienced
- Biotinidase DeficiencyDr. De Castro Pretelt isExperienced. Learn about Biotinidase Deficiency.
- Pyruvate Carboxylase DeficiencyDr. De Castro Pretelt isExperienced. Learn about Pyruvate Carboxylase Deficiency.
- Sudden Infant Death Syndrome (SIDS)Dr. De Castro Pretelt isExperienced. Learn about Sudden Infant Death Syndrome (SIDS).