DiGeorge syndrome || 22q11. 2 deletion syndrome || Immunodeficiency
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DiGeorge syndrome || 22q11. 2 deletion syndrome || Immunodeficiency
DiGeorge syndrome, also known as 22q11. 2 deletion syndrome, is a syndrome caused by the deletion of a small segment of chromosome 22. While the symptoms can vary, they often include congenital heart problems, specific facial features, frequent infections, developmental delay, learning problems and cleft palate.
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Do you know what DiGeorge Syndrome is? It’s a genetic disorder caused by a missing piece of a chromosome. 1 in 4,000 children have it, and that includes little Erick. But thanks to the tireless efforts of the RCMA staff at our Balm CDC, he is making great progress thanks to the nurturing that he needs to succeed despite his illness. THAT is what RCMA is all about. Every child deserves a chance! #rcmacares #digeorgesyndrome #rcma60 | RCMA
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Do you know what DiGeorge Syndrome is? It’s a genetic disorder caused by a missing piece of a chromosome. 1 in 4,000 children have it, and that includes little Erick. But thanks to the tireless efforts of the RCMA staff at our Balm CDC, he is making great progress thanks to the nurturing that he needs to succeed despite his illness. THAT is what RCMA is all about. Every child deserves a chance! #rcmacares #digeorgesyndrome #rcma60 | RCMA
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