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The card can be used to save up to $1,800 on Zepbound a year and may be used for up to 13 prescription fills in a calendar year. Worth noting: The card expires and the savings ends on December 31 ...
Zepbound, also sold under the brand name Mounjaro for type 2 diabetes, is part of a top-selling class of drugs designed to mimic the action of the GLP-1 hormone, which helps regulate blood sugar ...
Zepbound, like other GLP-1 agonists, can cause uncomfortable side effects, including gastrointestinal problems. According to the FDA’s drug label, side effects include: Nausea
Genetics of Down syndrome. Down syndrome is a chromosomal abnormality characterized by the presence of an extra copy of genetic material on chromosome 21, either in whole ( trisomy 21) or part (such as due to translocations ). The effects of the extra copy varies greatly from individual to individual, depending on the extent of the extra copy ...
The only factor that has been linked to the increased chance of having a baby with Down syndrome is advanced parental age. This is mostly associated with advanced maternal age but about 10 per cent of cases are associated with advanced paternal age. [94] Karyotype for Down syndrome (trisomy 21) showing the three copies of chromosome 21
Blue baby syndrome can refer to conditions that cause cyanosis, or blueness of the skin, in babies as a result of low oxygen levels in the blood. This term has traditionally been applied to cyanosis as a result of:. [ 1] Cyanotic heart disease, which is a category of congenital heart defect that results in low levels of oxygen in the blood. [ 2]
By Bhanvi Satija and Sneha S K. (Reuters) -All doses of Eli Lilly's weight-loss drug Zepbound and diabetes drug Mounjaro are now available, the U.S. Food and Drug Administration's updated shortage ...
The average IQ of a young adult with Down syndrome is 50, equivalent to the mental age of an 8- or 9-year-old child, but this number varies widely. [3] At the same time, they enjoy a rich social and emotional awareness. [4] Down syndrome is the most common chromosome abnormality in humans, [3] occurring in about one per 1000 babies born each ...