RP is a rare inherited blinding eye disease that affects about 1 in 4.

RP is a rare inherited blinding eye disease that affects about 1 in 4,000 people in the United States. It is believed that mutations in more than 100 different genes have been identified, only half caused.

Can be in a dry form by a build up of deposits on the retina and a wet form by the formation of abnormal blood vessels in the leak and the delicate retinal tissue to be caused.

The study, 8th Online August published in the Proceedings of the National Academy of Sciences Early Edition, has been suggesting that the mutation is a significant cause of RP in people of Jewish descent to be. The results also provide the basis for the development of prevention and treatment of this form of RP with a combination of genetic testing, gene therapy and cell replacement approaches..Most weight loss studies have noted that a highly low carbohydrate diet is not a good way to reduce weight. – She said that to low carbohydrate diet exacerbates which cravings for carbohydrates and slows metabolism As a result, after a short period of weight loss, there is a fast return to obese. Female of low-carbohydrate diets are successful after two years of, and most of them not deal addicted eat pulses, said Jakubowicz..

‘You emphasize the necessity of further studies, including cost-benefit comparisons surgical over surgical treat of solid C 2 fractures.. Source: The Endocrine Society.Submitted by: Catharine Paddock,vs Vs. Noninvasively treatment on neck fractures.

For earlier adults are with a C 2 from which have spinal surgical and non-surgical treatment similar short-and long term results, reports a study in the the May issue of from Neurosurgical, official magazine of Congress of Neurological Surgeons. The periodical is published by Lippincott Williams & Wilkins, part of from Wolters Kluwer Health.

There was no evidence that recent, healthier patients was more likely be subjected to an operation.