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Samantha Vergano, MD, Medical Genetics, Norfolk, VA, Children's Hospital of The King's Daughters

SamanthaAlexandraVerganoMDFAAP, FACMG

Medical Genetics Norfolk, VA

Clinical Genetics

Associate Professor, Pediatrics, Eastern Virginia Med Sch

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  • Office

    601 Childrens Ln
    Division Of Medical Genetics And Metabolism
    Norfolk, VA 23507
    Phone+1 757-668-9723
    Fax+1 757-668-9724
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Summary

  • Dr. Samantha Vergano is a medical geneticist in Norfolk, VA and is affiliated with multiple hospitals in the area, including Children's Hospital of The King’s Daughters and Sentara Norfolk General. She received her medical degree from Eastern Virginia Medical School and has been in practice 11 years. She specializes in clinical genetics and is experienced in intellectual disability, multiple congenital anomalies, dysmorphology, and inborn errors of metabolism.

Education & Training

  • Children's Hospital of Philadelphia
    Children's Hospital of PhiladelphiaResidency, Medical Genetics and Genomics, 2009 - 2012
  • Atlantic Health System/Goryeb Children's Hospital
    Atlantic Health System/Goryeb Children's HospitalResidency, Pediatrics, 2006 - 2009
  • Eastern Virginia Medical School
    Eastern Virginia Medical SchoolClass of 2006

Certifications & Licensure

  • VA State Medical License
    VA State Medical License 2012 - 2024
  • WA State Medical License
    WA State Medical License 2023 - 2024
  • NC State Medical License
    NC State Medical License 2020 - 2022
  • PA State Medical License
    PA State Medical License 2009 - 2012
  • NJ State Medical License
    NJ State Medical License 2007 - 2011
  • American Board of Pediatrics Pediatrics
  • American Board of Medical Genetics and Genomics Clinical Genetics and Genomics

Publications & Presentations

PubMed

Journal Articles

  • The ARID1B Spectrum in 143 Patients: From Nonsyndromic Intellectual Disability to Coffin–Siris Syndrome  
    Ellen R Elias, Kylin Lammers, Samantha A Vergano, John B Moeschler, Nature

Press Mentions

  • De Novo Loss-of-Function Variants in X-linked MED12 Are Associated with Hardikar Syndrome in Females
    De Novo Loss-of-Function Variants in X-linked MED12 Are Associated with Hardikar Syndrome in FemalesNovember 27th, 2020

Hospital Affiliations