Congenital Hearing Loss

klinefelter turner :: Article Creator Klinefelter Syndrome: Symptoms, Causes, Diagnosis, And Treatment - WebMD Klinefelter syndrome is a genetic condition in which a boy is born with an extra X chromosome. Instead of the typical XY chromosomes in men, they have XXY, so this condition is also called XXY syndrome. Men with Klinefelter usually don't know they have it until they run into problems trying to have a child. There's no cure, but doctors can treat it. You get the extra X chromosome by chance. Either the egg or the sperm that came together to create you had an extra X chromosome. Older women have a slightly higher chance of having a boy with XXY syndrome, but the chance is small. Men with Klinefelter may have: An extra X chromosome in every cell, which is the most common An extra X chromosome in only some cells, called mosaic Klinefelter, in which you don't have as many symptoms More than one extra X chromosome, whi...

turner syndrome is the result of :: Article Creator School Nurse Using Turner Syndrome Diagnosis To Inspire Others Your browser is not supportedtheleafchronicle.Com theleafchronicle.Com wants to ensure the best experience for all of our readers, so we built our site to take advantage of the latest technology, making it faster and easier to use. Unfortunately, your browser is not supported. Please download one of these browsers for the best experience on theleafchronicle.Com OpinionHow Turner Syndrome Inspired Me To Join The DI's DEI ... I joined The Daily Iowan's Diversity, Equity, and Inclusion Committee because I have an overlooked and poorly portrayed condition. Ally Pronina, Opinions ColumnistApril 18, 2021 Turner syndrome led me to one of the most impactful experiences. Having a medical condition that media organizations often overlook or misrepresent is what inspired me to join The Daily Iowan's Div...

if both parents are carriers for cystic fibrosis :: Article Creator Screening For Cystic Fibrosis Carriers - Health & Wellbeing by Peter Lavelle Every year 70 babies are born in Australia with cystic fibrosis, mostly to parents with no family history of this crippling illness. Experts are calling for more widespread screening for carriers. Published 01/12/2005 Every year, 70 babies are born in Australia with cystic fibrosis. The child suffers serious lung and digestive problems - they don't manufacture a vital protein, which causes secretions to become very sticky and their lungs and pancreas to literally 'gum up'. The lungs become susceptible to infection and digestion doesn't work properly. Treatment is much more effective than it was 20 years ago. Most children with cystic fibrosis now can expect to survive into adulthood. But the average life expectancy is still only in the mid thirties. Cystic fibrosis is a...

blood cancer polycythemia :: Article Creator Rusfertide Earns Breakthrough Therapy Designation In Polycythemia Vera The FDA has granted rusfertide breakthrough therapy designation for patients with polycythemia vera, a step that could speed its path to approval. The FDA granted rusfertide breakthrough therapy designation for patients with polycythemia vera. An investigational drug called rusfertide may soon offer a new treatment option for people living with polycythemia vera, a rare blood cancer that causes the body to produce too many red blood cells. Protagonist Therapeutics announced that the U.S. Food and Drug Administration (FDA) has granted rusfertide breakthrough therapy designation, a step that could speed its path to approval. This designation adds to rusfertide's earlier orphan drug and fast track statuses, all of which provide regulatory advantages designed to help new therapies reach patients more quickly. In the new...