Seizure In Shower Emergency & Heart Event #22q
Seizure In Shower Emergency & Heart Event #22q Welcome To Autism Insights :) I'm Dyan, I Live in Perth Australia. I'm an Aussie autistic vlogger, vlogging my life. I have a very difficult rare challenging syndrome 22q11.2 Deletion Syndrome, a genetic chromosomal syndrome. 22q is the genetic cause for my autism and many more struggles. I'm level-2 Autistic ASD, Moderate IDD, Genetic Seizures (SYNGAP1 Gene, rare form of seizures) ADHD, HSAM (Highly Superior Autobiographical Memory), Tourette's & OCD, one of my autistic special interests is Psychology and my faith. My hubby is level-1 autistic. He is my guardian who helps me to be independent due to my intellectual disability. I love my autism quirks and they seem to make people laugh. A 22q life is short so I like to have fun as much as I can. I'm cheeky and like to push the boundaries. Dancing is my favourite stim! Please join our community and become friends, we would love you to Subscribe! It is a safe community for all. I hope you enjoy our vlogs, welcome :) Tonic-clonic seizures, often generalized, occur in about 7–21% of individuals with 22q11.2 deletion syndrome, often linked to neonatal or chronic hypocalcemia, structural brain abnormalities (e.g., cortical dysplasia), or lowered seizure thresholds. These seizures typically respond well to standard anti-seizure medications. Causes: Hypocalcemia: A major factor due to parathyroid dysfunction (hypoparathyroidism) leading to low calcium, especially in the neonatal period or later due to hypocalcemia-induced seizure. Structural Brain Abnormalities: Issues like polymicrogyria, periventricular nodular heterotopia, or cortical dysplasia. Other Factors: Lowered seizure thresholds and, in adults, increased susceptibility to seizures induced by medications, such as antipsychotics or antidepressants. Dystonia is a recognized, often underdiagnosed, neurological movement disorder in 22q11.2 deletion syndrome (22q11.2DS), typically presenting with mild to moderate, action-related symptoms. It is considered part of the neurodevelopmental phenotype of 22q11.2DS, and is sometimes associated with earlier-onset Parkinsonism or, in rare, severe cases, structural issues manageable with deep brain stimulation (DBS). #22q #seizure #seizurevmanagement #emergency #emergencyresponse

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