Dr. Frances Kendall, MD
Clinical Biochemical Genetics ·
Female ·
Age 58
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Dr. Frances Kendall, MD is a clinical biochemical geneticist in Atlanta, GA and has been practicing for 25 years. She graduated from Rutgers Med Sch-Umdnj in 1987 and specializes in clinical biochemical genetics, medical genetics, and more.Read her story
Virtual Medical Practice, LLC
5579 Chamblee Dunwoody Rd Ste 110
Atlanta, GA 30338
(404) 793-7800
Insurance Accepted
- We do not accept health insurance
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Dr. Kendall's Experience
Dr. Kendall's experience matches your search based on the following criteria:
- Based on total number of patients treated over the last 12 months
- Specializes in Clinical Biochemical Genetics
- Board certified in Clinical Biochemical Genetics and Pediatrics
- No malpractice claims found
- No sanctions found
- No board actions found
Dr. Kendall's bio
This content was provided by Dr. Kendall "Dr Fran Kendall is 100% focused on patient care for children & adults from around the world with rare genetic, metabolic, mitochondrial & inherited disorders."
Care Philosophy
This content was provided by Dr. Kendall "We treat our patients they way we would want to be treated if the roles were reversed. Simple, but seems to be very powerful as our patient testimonials reflect."
4 Specialties
- Clinical Biochemical Genetics
- Clinical Genetics
- Medical Genetics
- Pediatric Medical Genetics
2 Board Certifications
- Clinical Biochemical GeneticsAccredited by: American Board of Medical Genetics*
- PediatricsAccredited by: American Board of Pediatrics*
48 Conditions Treated
- Adrenoleukodystrophy, Autosomal, Neonatal Form
- Angelman Syndrome
- Arginase Deficiency
- Arginine-Glycine Amidinotransferase Deficiency
- Arginninosuccinic Acid Synthetase Deficiency
- Autism
- Biotinidase Deficiency
- Canavan Disease
- Carbamoyl - Phosphate Synthase 1 Deficiency
- Carbohydrate Deficiency Glycoprotein Syndrome, Type II
- Carnitine Deficiency
- Carnitine Transport Deficiency
- Carnitine-Acylcarnitine Translocase Deficiency
- Citrulline Transport Defect
- Citrullinemia
- Citrullinemia II
- Drug-Induced Myopathies
- Duchenne Muscular Dystrophy
- Fabry's Disease
- Fragile X Syndrome
- Galactosemia
- Genetic Diseases
- Glucocerebrosidase Deficiency
- Glycogen Storage Disease
- Hemochromatosis
- Homocarnosinosis
- Inborn Errors of Metabolism
- Krabbe Disease
- Late-Onset Argininosuccinase Lyase Deficiency
- Late-Onset Citrullinemia
- Leigh Syndrome
- McArdle Disease
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- MELAS
- Menkes Disease
- Metabolic Disorders
- Metabolic Myopathies
- Metachromatic Leukodystrophy
- Methylmalonic Academia
- Mitochondrial Diseases
- Mitochondrial Encephalomyopathy - Aminoacidopathy
- Mitochondrial Myopathy - Lactic Acidosis
- Mitochondrial Neurogastrointestinal Encephalopathy Syndrome
- Mitochondrial Trifunctional Protein Deficiency
- Neonatal Argininosuccinase Lyase Deficiency
- Pompe Disease
- von Gierke's Disease
- X-Linked, Angelman-Like Syndrome
Less
1 Procedures
- Physical Examination
Background Check
0 Malpractice Claims
No malpractice history found for Georgia.
0 Sanctions
No sanctions history found for the years that Healthgrades collects data.
0 Board Actions
No board actions found for the years that Healthgrades collects data.
Education
- Temple UniversityUndergraduate School | Graduated 1982
- Rutgers Med Sch-UmdnjMedical School | Graduated 1987
- Harvard Medical Genetics Training Program (Children's Hospital Boston, Massachusetts Hospital and Massachusetts General Hospital)Fellowship Hospital | Completed 1993
Awards & Recognition
Awards & Honors
- Healthgrades Honor Roll
Media & Publications
- Braving the Pain, Nov, 2008
- Neonatal Renal Abscess Caused By Staphylococcus Aureus, 1991
- Metabolic Testing in Mitochondrial Disease, 2001
- Spectrum of phenotypic variability in Niemann-Pick type C disease: A cause of delayed diagnosis, 1998
- Legion of Mercy, Dec, 1996
- Present Newborn Screening for Phenylketonuria (PKU), 1999
- Mucopolysaccharidoses, 2006
- Familial recurrence of atypical symptoms in an extended pedigree with the syndrome of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS)., 1994
Languages Spoken
- English
Memberships & Professional Affiliations
Dr. Kendall does not have any memberships or affiliations listed. If you are Dr. Kendall and would like to add memberships or affiliations, please update your profile.
Dr. Kendall's Reviews
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Average Wait Time
- 10 – 15 minutes
Dr. Kendall's Performance
Office & Staff Performance
What People Say About Dr. Frances Kendall, MD
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I flew across the country to see Dr. Kendall and it was worth every penny of expense. By the time most of doctor Kendall’s patients get to her they have been through a gauntlet of misdiagnosis and unsatisfactory medical appointments. I believe that Dr. Kendall’s expertise and authentic...Read More
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1Karmen in Brainerd – Aug 27, 2018
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Dr Kendall is by far one of the most helpful and knowledgeable doctors I've seen in my life. She listened very attentively, answered all my questions, didn't talk down to me or dismiss my concerns. She readily recognized symptoms I hadn't even known to check for and gave referrals for treatment.
I...Read More
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2Amanda in Americus – Jul 07, 2017
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Dr. Kendall is truly an expert in h field and is very thorough. She takes time to review records, talk with families and patients and help guide them throughout whatever diagnosis they are facing. Scheduling has never been a problem, she has wonderful bedside manner and is really great with...Read More
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7Shelly in Brainerd, MN – Aug 10, 2016
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She was the best, she understood my dilemma and she didn't dismiss my symptoms. She listened , examined me and explained everything. Now I have a better understanding of what happened to me.
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73Dee. winfrey in 113 Orchard Dr Griffin Ga 30223 – Jan 22, 2016