Triple X syndrome, also called trisomy X or 47,XXX, is a genetic disorder that affects about 1 in 1,000 females. Females normally have two X chromosomes in all cells — one X chromosome from each parent. In triple X syndrome, a female has three X chromosomes. #triplexsyndrome #triplex #femalesyndrome #chromosome #genetics #genomicsforall #MiBiome #mibiometherapeutics
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Genetic testing can be useful to identify the underlying cause of epilepsy and to inform prognosis, optimal treatment, management, and risk of recurrence. Refer to the ARUP Consult Comprehensive Epilepsy Panel Test Fact Sheet to learn more about our new genetic test. https://bit.ly/3PIYPFl
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June 22nd is Rare Chromosome Disorder Awareness Day. It’s a day to celebrate, educate, shine bright together and reach out to those who need help or might not have heard of chromosome and gene disorders. "Share Your Colours!" is the theme for this year. Genetic testing can help you learn more about the likelihood of experiencing a genetic disorder. #rarechromosomedisorderawarenessday #ShareYourColours #genetictesting #geneticcounseling
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Day 6 of #SickleCellAwarenessMonth Sickle Cell Disease is an inherited haemoglobinopathy. This makes it both a genetic disorder and haematological disorder. Today we explain the genetics of Sickle Cell Disease. #sicklecelldisease #sicklecellawareness #sicklecell #geneticdisorders #haemoglobinopathies
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Hemochromatosis is a genetic disorder causing iron overload, but we can make a difference together. Join us in educating, supporting, and advocating for those with hemochromatosis as we strive for early detection, effective treatment, and improved quality of life. To learn more about how genetics plays a factor and how to detect signs early, visit https://bit.ly/3PFkMWl 💪💙 #HemochromatosisAwareness #EmpoweringLives
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