Paige Kaplan, MB, BCh

Paige Kaplan, MB, BCh, is a metabolic physician at The Children's Hospital of Philadelphia.

Areas of Expertise: Connective tissue disorders (Marfan syndrome, Osteogenesis Imperfecta, Ehlers Danlos syndromes, cutis laxa, osteoporosis in children), Inborn errors of metabolism including lysosomal disorders, especially Gaucher disease, Williams syndrome
Locations: Main Campus
Phone: 215-590-3376

  • Education and Training

    Medical School

    University of Witwatersrand, Johannesburg, South Africa

    Residency

    Montreal Children's Hospital, McGill University, Montreal, Canada

    Fellowship

    Montreal Children's Hospital, McGill University, Montreal, Canada

    Board Certification

    American Board of Pediatrics
    CCMG Canadian College of Medical Genetics
    Founding fellow, American College of Medical Genetics

  • Titles and Academic Titles

    Metabolic physician

  • Centers and Programs
  • Research Interests

    Clinical research in lysosomal disorders
    Inborn errors of metabolism
    Williams Syndrome

  • Publications

    Papers

    Sampson MG, Coughlin CR 2nd, Kaplan P, Conlin LK, Meyers KE, Zackai EH, Spinner NB, Copelovitch L. Evidence for a recurrent microdeletion at chromosome 16p11.2 associated with congenital anomalies of the kidney and urinary tract (CAKUT) and Hirschsprung disease. Am J Med Genet A. 2010 Oct;152A(10):2618-22. Read abstract.

    Collins RT 2nd, Aziz PF, Gleason MM, Kaplan PB, Shah MJ. Abnormalities of cardiac repolarization in Williams syndrome. Am J Cardiol. 2010 Oct 1;106(7):1029-33. Epub 2010 Aug 11. Read abstract.

    Collins RT 2nd, Kaplan P, Somes GW, Rome JJ. Long-term outcomes of patients with cardiovascular abnormalities and Williams syndrome. Am J Cardiol. 2010 Mar 15;105(6):874-8. Read abstract

    Collins RT 2nd, Kaplan P, Rome JJ. Stenosis of the Thoracic Aorta in Williams Syndrome. Pediatr Cardiol. 2010 Apr 22. [Epub ahead of print]. Read abstract