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As evident from the above discussions, researchers have mostly correlated the cellular radiosensitivity with the GPx activity level which is majorly contributed by GPx1 (because of its higher abundance) [1, 8, 9]

Now, building on proof-of-concept case reports toward structured clinical trials, next-generation strategies are advancing

Some of the most common ones are: poor muscle tone, called hypotonia, and feeding difficulties in infancy short stature and small hands or feet insatiable appetite, known as hyperphagia, starting in childhood, and leading to obesity motor developmental delay learning and speech difficulties sleep disturbances mood and behavioral problems, like temper outbursts and stubbornness underdeveloped sex organs, delayed puberty, and infertility Other possible symptoms include: distinct facial features, including almond-shaped eyes, a narrow forehead, and a downturned mouth thick saliva and tooth issues orthopedic issues such as scoliosis, an abnormal spine curvature unusually light skin, hair, and eyes body temperature regulation issues crossed eyes reduced sensitivity to pain Prader-Willi syndrome diagnosis PWS is first suspected when an infant, child, or teenager shows age-specific clinical features of the disease

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