De Vivo disease
De Vivo disease is an autosomal dominant developmental disorder associated with a deficiency of GLUT1.
Tags: genetic disorders
Ketogenic diet helps control the seizure by providing ketones as an alternative fuel to the brain instead of glucose.[
In rodent in vivo studies, chrysin was found anxiolytic.[21] [22] In herbal medicine, chrysin is recommended as a remedy for anxiety[23], but there are no controlled data in humans available. Many herbal remedies that contain chrysin tout their value as a libido-increasing supplement. There is no evidence so far in vivo. Chrysin demonstrated cell toxicity and inhibition of DNA synthesis at very low concentrations in a normal trout liver cell line.[24]
CSF glucose value, (<2.2 mmol/L), or lowered CSF/plasma glucose ratio( <0.4), erythrocyte 3-O-methyl-d-glucose uptake assay.
Children with this disease present with refractory seizure disorder, ataxia, and developmental delay with deceleration of head growth and microcephaly. The seizures are infantile, onset often beginning at 1-4 months of age, usually as complex seizures and later in childhood becoming more generalized. The frequency of seizures is variable and a history of decreasing seizure frequency during times of ketosis (ex: during an illness) may prompt the diagnosis. Developmental delay is global and includes receptive and expressive language dysfunction.
Immunology is a broad branch of biomedical science that covers the study of all aspects of the immune system in all organisms. It deals with, among other things, the physiological functioning of the immune system in states of both health and disease; malfunctions of the immune system in immunological disorders (autoimmune diseases, hypersensitivities, immune deficiency, transplant rejection); the physical, chemical and physiological characteristics of the components of the immune system in vitro, in situ, and in vivo. Immunology has applications in several disciplines of science, and as such is further divided.
Alzheimer's Disease Amyotrophic Lateral Sclerosis (ALS), e.g., Lou Gehrig's Disease Parkinson's Disease Niemann Pick disease Atherosclerosis Cancer Diabetes Heart Disease Inflammatory Bowel Disease (IBD) Norrie disease Prostatitis Osteoarthritis Osteoporosis Shy-Drager syndrome Rheumatoid Arthritis
Occurrence of an abundance of polyphenol antioxidants is associated with several salutary effects in higher animal species: Reduction in inflammatory effects such as coronary artery disease[2][3] including specific medical research into the pathways of improved endothelial health via downregulation of oxidative LDL.[4] More generally the tea polyphenol (medically known as TP) antioxidant epigallocatechin gallate, has been shown to reduce reactive oxygen species levels in vivo.[5] Reactive oxygen species are important markers for inflammatory diseases. Some polyphenol antioxidants, such as resveratrol, inhibit occurrence and/or growth of mammalian tumors.[6] A variety of other beneficial health effects have been attributed to consumption of foods rich in polyphenolic
Fabry disease (also known as Anderson-Fabry disease, Angiokeratoma corporis diffusum, Ruiter-Pompen-Wyers syndrome, Ceramide trihexosidosis, and Sweeley-Klionsky disease) is an X-linked recessive (inherited) lysosomal storage disease. The disease is named for Johannes Fabry.[1
Cognitive therapy is a widely accepted form of treatment for most anxiety disorders.[5] It is also thought to be particularly effective in combating disorders where the patient doesn’t actually fear a situation but, rather, fears what could result from being in said situation.[6] The ultimate goal of cognitive therapy is to modify distorted thoughts or misconceptions associated with whatever is being feared; the theory is that modifying these thoughts will decrease anxiety and avoidance of certain situations.[7] For example, cognitive therapy would attempt to convince a claustrophobic patient that elevators are not dangerous but are, in fact, very useful in
Neuropsychological screening tests, such as the mini-mental state examination (MMSE), are widely used to evaluate the cognitive impairments needed for diagnosis. More comprehensive test arrays are necessary for high reliability of results, particularly in the earliest stages of the disease.[88][89] Neurological examination in early AD will usually provide normal results, except for obvious cognitive impairment, which may not differ from standard dementia. Further neurological examinations are crucial in the differential diagnosis of AD and other diseases.[4] Interviews with family members are also utilised in the assessment of the disease. Caregivers can supply important information on the daily living abilities, as