Individuals with sickle cell disease (SCD) can live into their 40s, 50s, or longer with proper medical care, including regular check-ups, pain management, and preventive treatments. Advances in treatment, such as hydroxyurea and blood transfusions, have improved life expectancy significantly. However, complications can vary greatly among individuals, affecting overall health and longevity. Early diagnosis and comprehensive care are crucial for enhancing quality of life and lifespan.
people (girls/women) with turner syndrome live as long as regular people do....turner syndrome does not affect life spancy
Brett Sickler was born in 1983.
people with ushers syndrome will have a normal life expectancy
They live normal, long, healthy lives. The syndrome has been in my family for generations, and many live 85 years ore longer.
Charles Sickler was born on June 17, 1898, in Oklahoma, USA.
people can live up to 60 to 70 years.
Charles Sickler died on January 17, 1975, in Los Angeles, California, USA.
less than 30 years
16 years
50 to 60 years of age
Mae Conrad Sickler has written: 'Pioneer years in the Yakima Valley' -- subject(s): Frontier and pioneer life
People with Angelman Syndrome usually have a normal life span unless they have it severe or a bad rare kind of it. This can be followed up by looking for the symptoms.