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Results 11 - 20 of 33 for "22q11.2" deletion syndrome
  1. Learning about Velocardiofacial Syndrome From the National Institutes of Health (National Human Genome Research Institute)  
    Parathyroid Disorders/Genetics ... Parathyroid Disorders ... Cleft Lip and Palate/Specifics ... Cleft Lip and Palate ... Congenital Heart Defects/Specifics ... Congenital Heart ...
    https://www.genome.gov/Genetic-Disorders/Velocardiofacial-Syndrome - External Health Links
  2. Polymicrogyria 
    ... intellectual disability and multiple birth defects. These include 22q11.2 deletion syndrome, Adams-Oliver syndrome, Aicardi syndrome, Galloway-Mowat syndrome, ...
    https://medlineplus.gov/genetics/condition/polymicrogyria - Genetics
  3. Parathyroid Hormone (PTH) Test: MedlinePlus Medical Test 
    ... genetic disorders , such as DiGeorge syndrome, also called 22q11.2 deletion syndrome Getting too much vitamin D and/or calcium ...
    https://medlineplus.gov/lab-tests/parathyroid-hormone-pth-test - Medical Tests
  4. Critical congenital heart disease 
    ... conditions, such as Down syndrome, Turner syndrome, and 22q11.2 deletion syndrome, result from changes in the number or structure ...
    https://medlineplus.gov/.../critical-congenital-heart-disease - Genetics
  5. Pierre Robin Syndrome (Nemours Foundation)  
    ... ear infections, hearing problems, PRS, Stickler syndrome, 22q11 deletion syndrome, Treacher-Collins syndrome, continuous positive airway pressure, CPAP, NICU, polysomnography, sleep study
    https://kidshealth.org/en/parents/pierre-robin-syndrome.html - External Health Links
  6. Schizophrenia 
    ... palate), and are diagnosed with a condition called 22q11.2 deletion syndrome. AKT1 COMT YWHAE chromosome 22 Additional Information from ...
    https://medlineplus.gov/genetics/condition/schizophrenia - Genetics
  7. B and T cell screen 
    ... count may be due to: Chronic lymphocytic leukemia DiGeorge syndrome Multiple myeloma Waldenström macroglobulinemia A decreased T cell ...
    https://medlineplus.gov/ency/article/003329.htm - Medical Encyclopedia
  8. Double Outlet Right Ventricle (DORV) (Nemours Foundation)  
    Congenital Heart Defects/Specifics ... Congenital Heart Defects ... Nemours Foundation ... heart defect, congenital heart defect, atrium, atria, ventricles, VSD, double ...
    https://kidshealth.org/en/parents/dorv.html - External Health Links
  9. 22q11.2 duplication 
    ... Heine-Suner D. Mutations in TBX1 genocopy the 22q11.2 deletion and duplication syndromes: a new susceptibility factor for mental retardation. Eur J Hum Genet. 2007 Jun;15(6):658-63. doi: 10.1038/sj.ejhg.5201819. Epub 2007 Mar 21. ... variability of the 22q11.2 duplication syndrome. Eur J Med Genet. 2008 Nov- ...
    https://medlineplus.gov/genetics/condition/22q112-duplication - Genetics
  10. Overview of Immunodeficiency Disorders (Merck & Co., Inc.)  
    Immune System and Disorders/Specifics ... Immune System and Disorders ... Merck & Co., Inc. ... Overview of Immunodeficiency Disorders - Explore from the Merck Manuals - Medical ...
    https://www.merckmanuals.com/...erview-of-immunodeficiency-disorders - External Health Links
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