1p36 chromosome deletion syndrome...#sunblood #eyeamnotblack #Neuromelanin #starfamily #stemcells #DNA #starseeds #genetics #biology #blackbodyradiation | Kali Ma'at Cooper
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1p36 chromosome deletion syndrome...#sunblood #eyeamnotblack #Neuromelanin #starfamily #stemcells #DNA #starseeds #genetics #biology #blackbodyradiation | Kali Ma'at Cooper
164 views6 months ago
FacebookKali Ma'at Cooper
22q11.2 Deletion Syndrome Overview
22q11.2 Deletion Syndrome Overview
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22q Deletion Syndrome
22q Deletion Syndrome
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Microdeletion syndrome definition, causes, symptoms, diagnosis, treatment & prognosis
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18q deletion syndrome, causes, symptoms, diagnosis, treatment & life expectancy
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healthjade.net
Ten-year-old Gracie has Chromosone 1 deletion syndrome and complex needs. A recent endoscopy revealed an infection on Gracie’s lungs which her doctors fear may have caused some long term damage so she’s currently on antibiotics and needs lung rehabilitaion. Blowing bubbles helps Gracie rehab her lungs, it helps clear secretions, improve lung expansion, builds breathing strength,and regulates breathing and oxygenation. To begin with, the nebuliser was terrifying for Gracie. She was petrified it w
0:57
Ten-year-old Gracie has Chromosone 1 deletion syndrome and complex needs. A recent endoscopy revealed an infection on Gracie’s lungs which her doctors fear may have caused some long term damage so she’s currently on antibiotics and needs lung rehabilitaion. Blowing bubbles helps Gracie rehab her lungs, it helps clear secretions, improve lung expansion, builds breathing strength,and regulates breathing and oxygenation. To begin with, the nebuliser was terrifying for Gracie. She was petrified it w
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FacebookNoah's Ark Children's Hospital Charity
Jocelyn lives with a rare genetic disorder known as chromosome 8p deletion. She also enjoys life, family, and her loyal dog named Honey. Jocelyn wants others to know that she loves and cares about them. | Special Books by Special Kids
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Jocelyn lives with a rare genetic disorder known as chromosome 8p deletion. She also enjoys life, family, and her loyal dog named Honey. Jocelyn wants others to know that she loves and cares about them. | Special Books by Special Kids
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FacebookSpecial Books by Special Kids
What Is 1Q21.1 Microdeletion? Details on Gypsy Rose Blanchard’s Genetic Condition
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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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