Prader-Willi syndrome is a rare genetic disease that causes poor feeding in infancy but later triggers insatiable hunger.

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Discover how hemophilia A affects blood clotting, its genetic patterns, warning signs, advanced treatment options, and ...

Although we are exposed to the sun all year round, a surprising number of Malaysians have insufficient vitamin D, the ...

There’s a small takeout place on El Cajon Boulevard, not far from San Diego State, that serves delicious baskets of fried ...

Across decades of action cinema, from big budget blockbusters to transgressive B-movie fare, there exist the greatest fight ...

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5% among preterm infants and 9% among full-term infants. -Preterm and low-birthweight infants were seven times more likely to be admitted than other infants. Low birthweight is defined as 5.5 ...

Caused by a tiny fluke of nature—a mutation in a gene known as a SYNGAP1—the non-hereditary condition can lead to intellectual disabilities, epilepsy, autism spectrum disorder, insomnia, hypotonia ...

Additional characteristics of PWS include behavioral problems, cognitive disabilities, low muscle tone, short stature (when not treated with growth hormone), the accumulation of excess body fat, ...