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Typical absence seizure
- ... clearly Unaware of the seizure Specific symptoms of typical absence seizures may include: Changes in muscle activity, such as ...
- Landau-Kleffner Syndrome (Genetic and Rare Diseases Information Center)Genetic and Rare Diseases Information Center ... Aphasia/Children ... Aphasia ... From the National Institutes of Health ... Find symptoms and other information about Landau- ...
- Mitochondrial Disorders (National Institute of Neurological Disorders and Stroke)National Institute of Neurological Disorders and Stroke ... Neuromuscular Disorders/Specifics ... Neuromuscular Disorders ... Muscle Disorders/Specifics ... Muscle Disorders
- Leigh Syndrome (National Institute of Neurological Disorders and Stroke)National Institute of Neurological Disorders and Stroke ... Degenerative Nerve Diseases/Specifics ... Degenerative Nerve Diseases ... Genetic Brain Disorders/Specifics
- Mitochondrial DNA Depletion Syndrome (Alpers' Disease) (National Institute of Neurological Disorders and Stroke)National Institute of Neurological Disorders and Stroke ... Mitochondrial Diseases/Specifics ... Mitochondrial Diseases ... Degenerative Nerve Diseases/Specifics ... Degenerative ...
- ... eyes to the brain (the optic nerves) and seizures may also occur in this ... delayed development of the typical signs of puberty, such as the growth of ...
- Herpes Simplex Virus (HSV) in Infants (VisualDX)VisualDX ... Herpes Simplex/Children ... Herpes Simplex ... Herpes infections are caused by both herpes simplex virus type 1 (HSV-1) and herpes simplex virus type 2 (HSV- ...
- ... in this condition, and some affected individuals develop seizures.In vitamin D-dependent rickets, there is an ... hyperparathyroidism. Hypocalcemia can also cause muscle weakness and seizures in individuals with vitamin D-dependent rickets. Certain ...
- Amnesia (Mayo Foundation for Medical Education and Research)Mayo Foundation for Medical Education and Research ... Memory/Specifics ... Memory
- ... form may also have other signs and symptoms typical of MVA syndrome type 1. MVA syndrome is ... protein, and TRIP13 gene mutations lead to an absence of TRIP13 protein in cells. Without BUBR1 or ...