Michael & Jaxon were diagnosed with a rare chromosome disorder called 15q11.2 deletion at the age of 2 years old. Although we’ve come a long with research, there is still a lot more to learn about 15q11.2 deletion. @unique_charity are my go to when it comes to a better understanding of how the deletion is affecting my boys. What we know so far is that although Michael & Jaxon are diagnosed autistic, we feel that 15q11.2 is a contributing factor around their speech delay, their development delay,
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Michael & Jaxon were diagnosed with a rare chromosome disorder …
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ASAD KHAN on Instagram: "DiGeorge Syndrome (22q11.2 Deletion Syndrome) A genetic microdeletion syndrome causing **defects in structures derived from the 3rd and 4th pharyngeal pouches**. * **Main Cause:** **Microdeletion at chromosome 22q11.2** (autosomal dominant). * **Key Presentations (CATCH-22):** * **C**ardiac defects (Tetralogy of Fallot, truncus arteriosus) * **A**bnormal facies * **T**hymic aplasia → **T-cell deficiency** (recurrent viral/fungal infections) * **C**left palate * **H**ypoc
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