About Amel Karaa, MD

Amel Karaa, MD is a Board-certified internist and medical geneticist, who dedicated her professional life to treating patients with complex medical conditions by providing excellent clinical care, and therapeutics opportunities for those with mitochondrial and lysosomal storage disorders. She has established a specialized program evaluating hundreds of national and international patients.   Dr. Karaa is the 2013 United mitochondrial disease foundation (UMDF) fellow, a site investigator for the NIH North American Mitochondrial Disease Consortium (NAMDC), on the scientific/medical board of the UMDF, medical board of the national advocacy group MitoAction, multiple medical boards for different lysosomal storage disorders and as of June 2018, the elected president of the Mitochondrial Medicine society (MMS). 

 

Clinical Interests:

Treats:

Languages:

Locations

Genetic's Unit Administrative office
175 Cambridge street,
Boston, Massachusetts 02114
617-726-1561
Fax: 617-726-1566

Pediatric Genetics Clinic (Main MGH Hospital)
55 Fruit Street
Boston, MA 02114-2696
617-726-1561
Fax: 617-726-1566

Mass General/North Shore Center for Outpatient Care
102 Endicott Street
Danvers, MA 01923-3623
978-882-6999

Medical Education

  • MD, Universite de Medecine et de Pharmacie de Tunis
  • Residency, Mount Auburn Hospital
  • Fellowship, Boston Children's Hospital

American Board Certifications

  • Internal Medicine, American Board of Internal Medicine
  • Clinical Genetics (M.D.), American Board of Medical Genetics

Accepted Insurance Plans

Note: This provider may accept more insurance plans than shown; please call the practice to find out if your plan is accepted.


Research

As a clinician-scientist, Dr. Karaa endeavored to provide excellent clinical care, and therapeutics opportunities for patients with mitochondrial and lysosmal diseases. She has established a specialized program to care for both patients populations that serves hudnreds of patients each year. Dr. Karaa has a strong national and international reputation as a clinical expert in Mitochondrial diseases. she is the 2013 United mitochondrial disease foundation (UMDF) fellow, site PI in the NIH North American Mitochondrial Disease Consortium (NAMDC), where she chairs the planning and implementation of new study task force and conducts research on trying to identify the molecular basis of patients with symptoms compatible with a mitochondrial disease. She is on the scientific/medical board of the UMDF, medical board of the national advocacy group MitoAction and as of June 2018, the upcoming president of the Mitochondrial Medicine society (MMS). Through the MMS, she has helped revise the guidelines for patients’ diagnosis and management for mitochondrial disease. Most recently, I was part of the founding and a board member of the mitochondrial care network (MCN) to develop and implement mitochondrial centers of excellence in the US as a collaborative effort between the MMS and the mitochondrial disease advocacy groups. Dr. Karaa has also been conducting clinical research on mitochondrial and lysosomal storage diseases and is a principal investigator and the lead on several clinical trials and multiple ongoing projects developing new outcome measure tools for mitochondrial and lysosomal storage disorders.

Publications

  • View my most recent publications at PubMed

    Select Publications

    • Karaa A, Goldstein A. The Spectrum of Clinical Presentation, Diagnosis and Management of Mitochondrial Forms of Diabetes. Pediatric Diabetes 2015 Feb;16(1):1-9. 
    • Zar-Kessler C, Karaa, A, et al. Gastrointestinal Manifestations of Fabry Disease in Childhood: The Necessity of Prompt Recognition. Therap Adv Gastroenterol 2016, 9(4):626-34. 
    • Koenig MK, Emrick L, Karaa A, et al. Recommendations for the management of Stroke-like episodes in Patients with Mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes. JAMA Neurology JAMA Neurol. 2016;73(5):591-594. 
    • Parikh S, Karaa A, Goldstein A, et al. Solid Organ transplantation in primary mitochondrial disease: Proceed with caution. Mol Genet Metab 2016, 18(3):178-84.
    • Karaa A, Kriger J, et al. Mitochondrial disease patient’s perception of dietary supplements. Mol Genet Metab. 2016. S1096-7192(16)30127-5. 
    • Parikh, A. Goldstein, A. Karaa et al. Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society. Genet Med. 2017 Dec;19(12). doi: 10.1038/gim.2017. 
    • Amel Karaa, Richard Haas, et al. Randomized Dose-Escalation Trial of Elamipretide in Adults with Primary Mitochondrial Myopathy. 2018 Mar 2. 
    • Amel Karaa, Ibrahim Elsharkawi, et al. Effects of mitochondrial disease/dysfunction on pregnancy: A retrospective study. Mitochondrion, 2018, ISSN 1567-7249.