Stroke is a serious medical condition that affects thousands of people around the world every year. It occurs when there is an interruption in the blood supply to the brain, which can lead to permanent damage and even death. Stroke is a leading cause of disability and death in adults, and it is important to …
Multiple sclerosis (MS) is a neurological disorder that affects the central nervous system, impairing the communication between the brain and other parts of the body. It is a chronic, debilitating condition with no known cure. People living with MS experience a wide range of symptoms, from mild to severe, and it can affect both physical …
Schizophrenia is a serious mental illness that affects approximately 1.1% of the population worldwide. It is characterized by hallucinations, delusions, disorganized thinking and behavior, and other cognitive difficulties. People with schizophrenia often have difficulty functioning in society due to their symptoms, which can lead to social isolation and unemployment. Despite its prevalence, there is still …
Down Syndrome is a genetic disorder caused by an extra copy of chromosome 21. This chromosomal abnormality affects physical and intellectual development, which can lead to a variety of health problems. People with Down Syndrome experience delays in motor skills, language, and cognitive development. They often have physical characteristics such as low muscle tone, short …
Turner Syndrome is a genetic disorder that occurs in females. It is caused by the complete or partial absence of a second sex chromosome, resulting in a chromosomal pattern of 45,X instead of the typical 46,XX or 46,XY. Turner Syndrome affects 1 in 2,500 female births and can cause physical, developmental and psychological issues. The …
Fragile X Syndrome is a genetic disorder that affects approximately 1 in 4,000 people, and is the most common inherited form of intellectual disability. It is caused by a mutation of the FMR1 gene on the X chromosome. This mutation leads to an abnormal number of repeats of a single nucleotide sequence within the gene, …
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