KAND patients experience many overlapping symptoms relating to muscle strength, coordination, reflexes, and balance. These symptoms may worsen over time as a result of degeneration, and increased strain as the body grows.

KAND is a group of rare neurological disorders in children caused by variants (mutations) in the KIF1A gene, which plays an important role in the nervous system. Children with KAND have developmental delays and varied neurological symptoms. Some forms of KAND are mild, while others can be life-threatening.

KIF1A Associated Neurological Disorder (KAND) is a progressive neurodegenerative disorder caused by mutations in the KIF1A gene. Learn about the disorder.

2017年5月14日 · KIF1A Associated Neurological Disorder (KAND) is a rare severe neurodevelopmental and neurodegenerative disease. KAND is caused by mutations in the KIF1A gene. There are currently over 100 identified mutations in the KIF1A gene. The symptoms and their severity vary depending on mutation type and individual patient.

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KIF1A associated neurological disorder (KAND) is caused by one or more disease-causing variations in the KIF1A gene. KIF1A is responsible for producing the KIF1A protein. This protein is, in turn, vital for the health of brain cells and nerve fibers.

2023年9月29日 · Learn about KIF1A-Related Disorder, including symptoms, causes, and treatments. If you or a loved one is affected by this condition, visit NORD to find.

KIF1A-associated neurological diseases (KANDs) are a group of inherited conditions caused by changes in the microtubule (MT) motor protein KIF1A as a result of KIF1A gene mutations. Anterograde transport of membrane organelles is facilitated by the kinesin family protein encoded by the MT-based motor gene KIF1A.

2024年8月9日 · KIF1A-associated neurological disorder (KAND) is a neurodegenerative and often lethal ultrarare disease with a wide phenotypic spectrum associated with...

KIF1A.ORG is a global community dedicated to improving the lives of those affected by KIF1A Associated Neurological Disorder (KAND) and accelerating research to find a cure. Newly Diagnosed? Register with our organization. February 28th is Rare disease Day, and this year we are celebrating with two important initiatives! 1.