It depends on the severity, the life style, and the level of medical care.
Males can live into their seventies, but the average is much lower ... mid-thirties is common.
Females (very rare) almost never live past their teens.
Traditional Hemophilia is present from birth and throughout the individual's life. This is because the disorder is genetically linked and genetics are pretty much set at the time of conception. Acquired Hemophilia, which is much more rare, can begin at pretty much any stage of an individual's life. While being more common in older people than younger, any person on certain medications, people with liver disease, and a handful of other situations can develop acquired hemophilia. (Acquired hemophilia is not inherited.)
Hemophilia is a genetic disease, therefore people who have ancestors who were hemophiliacs have a greater chance of getting it.
The life expectancy rate in Equatorial Guinea is around 64 years, according to the World Bank data.
Yes, hemophilia can be life-threatening if not managed properly. Excessive bleeding, especially internally or in the brain, can lead to serious complications or death. Regular medical supervision and treatment are essential for individuals with hemophilia to prevent severe bleeding episodes.
There is an inverse relationship between infant mortality rate and life expectancy - as infant mortality rate decreases, life expectancy tends to increase. This is because lower infant mortality indicates better overall health and access to healthcare in a population, which can lead to longer life expectancy. Improvements in infant survival rates often reflect improvements in overall healthcare and living conditions that benefit individuals at all stages of life.
Normal life expectancy, so long as you don't cut yourself severely.
Yes. Hemophilia is when the body cannot clot blood properly. Although technology has increased the life expectancy, it is entirely possible for a child or adult to die from this.
Hemophilia itself does not directly cause death; rather, it is a genetic disorder that affects blood clotting, leading to an increased risk of bleeding. Historically, individuals with severe hemophilia faced higher mortality rates due to complications from uncontrollable bleeding or infections. Advances in treatment, such as factor replacement therapy, have significantly improved life expectancy and quality of life for those with hemophilia. However, precise statistics on deaths specifically attributed to hemophilia can vary and are not easily quantified.
The life expectancy for Caymanians is the early 80's
Individuals with hemophilia can have a near-normal lifespan if they receive proper medical care and treatment. Advances in therapies, such as factor replacement and gene therapy, have significantly improved life expectancy and quality of life. However, complications from bleeding episodes and associated health issues can still impact longevity. Overall, with appropriate management, many people with hemophilia live well into adulthood and beyond.
People in Australia would expect to have a higher life expectancy than people in Africa. There are lots of very well developed parts of Africa where people would have a high life expectancy, but on average it would have a lower life expectancy.
The life expectancy in the United Kingdom is 78.85.
The life expectancy for Liberia is 38.9 male and 41.9 female.
The average life expectancy of people is higher than it was in the past. People who are homeless are known to have a lower life expectancy.
The life expectancy with someone with carcinoid lung cancer depends on the stage of the cancer. For people with stage 1, the life expectancy is 93%. For people with stage 5, the life expectancy is 57%.
The life expectancy for a someone in Cuba is about 77.08 years. Women have a slightly longer life expectancy than men in that island nation.
According to an average of life expectancy statistical charts, a person born in 1941 has a life expectancy of 62.81 years.