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Results 1 - 10 of 27 for Shprintzen syndrome
  1. Shprintzen-Goldberg syndrome is a disorder that affects many parts of the body. Affected individuals have a combination of distinctive facial features and skeletal ...
  2. ... these conditions DiGeorge syndrome, velocardiofacial syndrome (also called Shprintzen syndrome), and conotruncal anomaly face syndrome. In addition, some ...
  3. DiGeorge Syndrome (DGS) (American Academy of Allergy, Asthma, and Immunology)  
    An overview of DiGeorge Syndrome (DGS) symptoms, diagnosis, treatment and management written by experts in allergy, asthma and immunology. ... DiGeorge syndrome, DGS, primary immunodeficiency disease, PIDD, infections, T cell production and function, chromosome 22q11.2, chromosome 10p13, ...
  4. ... SKI gene have been found in people with Shprintzen-Goldberg syndrome, a condition characterized by distinctive facial features, skeletal ... the wide range of signs and symptoms of Shprintzen-Goldberg syndrome. More About This Health Condition proto-oncogene c- ...
  5. Cleft Lip and Palate/Specifics ... Cleft Lip and Palate ... Congenital Heart Defects/Children ... Congenital Heart Defects ... Immune System and Disorders/Children ... Immune ...
  6. What Are Related Conditions? (Marfan Foundation)  
    Marfan Syndrome/Related Issues ... Marfan Syndrome ... Marfan Foundation ... The Marfan Foundation's mission is to save lives and improve the quality of life of individuals ...
  7. Craniofacial Abnormalities (National Library of Medicine)  
    Craniofacial is a medical term that relates to the bones of the skull and face. Craniofacial abnormalities are birth defects of the face or head. Some, like cleft ...
  8. Immune System and Disorders (National Library of Medicine)  
    What is the immune system? Your immune system is a complex network of cells, tissues, and organs. Together they help the body fight infections and other ...
  9. ... or Free article on PubMed Central Baldini A. DiGeorge syndrome: an update. Curr Opin Cardiol. 2004 May;19( ... localization signal in Tbx1 that is deleted in DiGeorge syndrome patients harboring the 1223delC mutation. Hum Mol Genet. ...
  10. ... count may be due to: Chronic lymphocytic leukemia DiGeorge syndrome Multiple myeloma Waldenström macroglobulinemia A decreased T cell ...
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