Turner Syndrome is a chromosomal disorder where one or part of the sex chromosomes (X chromosomes) is missing. Turner Syndrome doesn't reduce the life expectancy of a person directly, so their life expectancy is about the same as the average person. However, they are often faced with health concerns such as Heart disease, Diabetes etc.
No
The same as everybody else really, except for not being able to reach high things and more medical appointments.
characterized by a slight intrauterine growth retardation, relatively normal growth rates for the first several years of life, a progressive deceleration of growth later in childhood, and the lack of a pubertal growth spurt.
Symptoms of Turner Syndrome may include any of the following:Short StaturePremature Ovarian FailureSpecific Heart problemsKidney problemsThyroid problemsHearing problems and a high number of ear infections during childhoodNLD (Nonverbal Learning Disorder) like behaviorADHD (Attention Deficit Hyperactivity Disorder) like behaviorOther Physical features of Turner may include:· Narrow, high-arched palate (roof of the mouth)· Retrognathia (receding lower jaw)· Low-set ears· Low hairline (the hair on the neck is closer to the shoulders)· Webbed neck (excess or stretched skin)· Slight droop to eyes· Strabismus (lazy eye)· Broad chest· Cubitus valgus (arms that turn out slightly at the elbows)· Scoliosis (curvature of the spine)· Flat feet· Small, narrow fingernails and toenails that turn up (usually if lymphedema was present at birth)· Short fourth metacarpals (the ends of these bones form the knuckles)· Edema (swelling) of hands and feet, especially at birth
The original answer here was "75 age", but that is highly unrealistic answer. The Charge Syndrome website talks about a 70% mortality rate before age 5. As charge is weakness of multiple vital organs which can fail anytime after that... even years later, no real estimate can be given. With improvements in healthcare the outlook can be positive. One case lived to be 52 years.
No
people (girls/women) with turner syndrome live as long as regular people do....turner syndrome does not affect life spancy
what is the life expentancy for individuals with cat cry syndrome
63 years
Normal
They cant exercise as vigorously as someone without Marfan syndrome
they are dwarfed and die young
As of October 2023, research on Turner syndrome continues to advance, focusing on various aspects such as genetic mechanisms, hormonal treatments, and long-term health outcomes. Studies are investigating the role of growth hormone and estrogen replacement therapies in improving quality of life and addressing associated health risks like cardiovascular disease and osteoporosis. Additionally, there is an emphasis on psychosocial support and early diagnosis to enhance management strategies for individuals with Turner syndrome. Ongoing genetic research aims to uncover further insights into the condition's complexities and potential therapeutic targets.
The life expectancy of someone with Job syndrome (Hyper-IgE syndrome) varies based on individual health and medical management. With proper treatment, such as antibiotics for infections and managing associated complications, many individuals with Job syndrome can live into adulthood. However, there can be a higher risk of certain complications that may affect life expectancy.
The average height for someone with Morquios syndrome will grow an average of four feet. The life expectancy can vary from four years to seventy years.
The same as everybody else really, except for not being able to reach high things and more medical appointments.
this is called turner syndrome. it is when females are missing their 2nd X chromosome. It only affects females because a male missing their X chromosome would only be a Y chromosome and that is fatal. Look turner syndrome up on wikipedia for more information.