Clinical Biochemical Geneticist focused on mitochondrial disorders, autism, and inborn errors of metabolism. Evaluation, diagnosis, ongoing management, biopsy, buccal swab, CMA, nuclear gene sequencing, next gen sequencing and whole exome gene sequencin

Medical Genetics

Frances Kendall practices Medical Genetics. She went to Rutgers New Jersey Medical School. Rutgers New Jersey Medical School is ranked 76 in research and 0 in primary care medicine She over the years received 1 awards: "Making a Difference in Mitochondrial Medicine". Frances Kendall is also published. She has 11 publications published. The lastest publication: "Familial recurrence of atypical symptoms in an extended pedigree with the syndrome of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS).'

Publications

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• Practice patterns of mitochondrial Disease physicians in North America. Part 2: treatment, care and management.
• Practice patterns of mitochondrial Disease physicians in North America. Part 1: Diagnostic and clinical challenges.
• MLYCD mutation analysis: evidence for protein mistargeting as a cause of MLYCD Deficiency.
• Metabolic testing in mitochondrial Disease.
• Rod photoreceptor function in children with mitochondrial disorders.
• MCT oil-based diet reverses hypertrophic cardiomyopathy in a patient with very long chain acyl-coA dehydrogenase Deficiency.
• Spectrum of phenotypic variability in Niemann-Pick type C Disease: A cause of delayed diagnosis.
• Mucolipidosis II (I-cell disease) presenting as Neonatal cholestasis.
• Familial recurrence of atypical symptoms in an extended pedigree with the Syndrome of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS).
• Neonatal renal abscess caused by Staphylococcus aureus.

Schools

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• Rutgers Med SchUMDNJ

• Harvard Medical Genetics Training Program Children39s Hospital Boston Massachusetts Hospital and Massachusetts General Hospital

• Temple University

Procedures Preformed

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• Physical Examination

Conditions Treated

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• Adrenoleukodystrophy, Autosomal, Neonatal Form
• Angelman Syndrome
• Arginase Deficiency
• Arginine-Glycine Amidinotransferase Deficiency
• View All

Doctors Specialties

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• Clinical Biochemical Genetics
• Clinical Genetics
• Medical Genetics
• Pediatric Medical Genetics

Accepted Insurances

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Awards

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• Making a Difference in Mitochondrial Medicine

Education

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• Boston Children's Hospital
• Tufts Medical Center
• Thomas Jefferson University
• Rutgers New Jersey Medical School

Hospital

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• Children's Healthcare of Atlanta

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