Skip to main content Skip to navigation
We care about your privacy. Read about your rights and how we protect your data. Get Details

COVID-19 Update:Learn more about how we are protecting our patients, families and staff, as well as other important facts about COVID-19.

22q Multidisciplinary Clinic

The Children’s National Hospital 22q Multidisciplinary Clinic provides specialized treatment services for children and adolescents with genetic differences caused by a missing or extra piece of chromosome 22.

Our program’s multidisciplinary approach means a variety of experts familiar with 22q are able to help your child through diagnosis and treatment with the best care possible. Families who have experienced 22q also share their advice and expertise with our teams when able.

22q Disorders

22q11.2 deletion syndrome (22q11.2 DS), also known as DiGeorge Syndrome or Velocardiofacial Syndrome, is the most common microdeletion syndrome and is many times underdiagnosed. This syndrome has a variable phenotype and affects multiple systems, making early recognition and multidisciplinary management imperative. This condition is characterized by congenital heart disease (especially conotruncal defects), immunodeficiency, hypoparathyroidism, palatal, gastrointestinal, skeletal and renal abnormalities. Characteristic facial features, developmental and speech delay, and an increased risk for psychiatric illness are also observed.

22q11.2 duplication is a condition caused by an extra copy of a small piece of chromosome 22. The duplication occurs near the middle of the chromosome at a location designated q11.2. The features of this condition vary widely, even among members of the same family. Affected individuals may have developmental delay, intellectual disability, slow growth leading to short stature, and weak muscle tone (hypotonia). Many people with the duplication have no apparent physical or intellectual disabilities.

22q Clinic Services 

Our team involves cardiology, ENT, audiology, immunology, psychology, endocrinology, plastic surgery and genetics specialists that have experience with 22q syndromes. We discuss and evaluate the information of our patients together in order to improve patient care and decrease the burden of several appointments on different days. All the providers offer in-person visits as well as telehealth evaluations.  

Contact Us

For more information or to engage with our services, contact us at 202-476-2187 or email Christine Lynn Maccia.

22q Clinic Team

  • Sarah Clauss

    Sarah Clauss
    Advanced Imaging Cardiologist

  • Tracey Ambrose

    Tracey Ambrose
    Lead Audiologist

  • Nadia Merchant M.D.

    Nadia Merchant

  • Eyby Leon Janampa

    Eyby Leon Janampa
    Medical Geneticist

  • Vanessa Bundy

    Vanessa Bundy

  • Diego Preciado

    Diego Preciado
    Division Chief, Ear, Nose, and Throat (Otolaryngology)
    Director, Pediatric Otolaryngology Fellowship
    Co-Director of the Cochlear Implant Program

  • Albert Oh

    Albert Oh
    Director, Cleft and Craniofacial Program
    Director, Plastic Surgery Fellowship
    Plastic and Reconstructive Surgeon

  • Ashley Ramos

    Ashley Ramos