Скачать или смотреть Seizure In Shower Emergency & Heart Event

Seizure In Shower Emergency & Heart Event #22q

Hi welcome to our YouTube Channel Ok Aussie Vlogger. Perth, Western Australia.

Dyan is an Aussie vlogger, vlogging her life's journey with a Genetic 22q11.2 Deletion Syndrome and all the co-existing conditions that come with 22q. I am Matt her hubby and full time carer for you carers, I share my carers experience, tips and helpful things I have discovered along the way.

Dyan Linley Moore is utilising YouTube to share her living journal and wants to connect, advocate and share with her community while also leaving behind a living journal for her family. Dyan has 22q with co-existing conditions
Dystonia
Genetic Seizures
ASD Classic Autism
ADHD
OCD
Tourette's Ehlers-Danlos
ME/CFS
Lyme Disease

22q.11.2 Deletion Syndrome is a life-threatening rare genetic chromosomal disorder. Average age life expectancy is 41. Dyan is a creative, a comedian and a vibrant person who loves life despite the challenges.

We would love you to join our community and Subscribe, Like and Share to others!

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