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DiGeorge syndrome
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- 22q11.2 Deletion Syndrome (DiGeorge Syndrome) (For Parents) (Nemours Foundation)22q11.2 deletion syndrome, genetic condition, DiGeorge syndrome, velocardiofacial syndrome (VCFS), Shprintzen syndrome, conotruncal anomaly face syndrome, Caylor cardiofacial syndrome, genetic, inherited, genes, genetic mutation, sindrome, syndrome, 22qDS, 22q, 22q11. ...
- 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, ...
- ... described as separate conditions. Doctors named these conditions DiGeorge syndrome, velocardiofacial syndrome (also called Shprintzen syndrome), and conotruncal ...
- ... 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. ...
- 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 ...
- ... count may be due to: Chronic lymphocytic leukemia DiGeorge syndrome Multiple myeloma Waldenström macroglobulinemia A decreased T cell ...
- Cleft Lip and Palate (National Library of Medicine)Cleft lip and cleft palate are birth defects that occur when a baby's lip or mouth do not form properly. They happen early during pregnancy. A baby can have ...
- Congenital Heart Defects (National Library of Medicine)What are congenital heart defects? Congenital heart defects (CHDs) are problems with the structure of the heart. "Congenital" means that that the problems ...
- ... caused by: Chromosome 18q deletion syndrome Cohen syndrome DiGeorge syndrome Oral-facial-digital syndrome (OFD)
- Learning about Velocardiofacial Syndrome (National Human Genome Research Institute)Parathyroid Disorders/Genetics ... Parathyroid Disorders ... Congenital Heart Defects/Specifics ... Congenital Heart Defects ... Cleft Lip and Palate/Specifics ... Cleft Lip and ...