الفهرس 
INTRODUCTIONOnly 14 pages are availabe for public view
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Abstract
There is no doubt that the childhood of the most important stages in human life, but some children are born premature births (premature) they shall be within days to the first months of life at risk for a wide range of complex diseases that threaten their growth and survival in life.
It was found that premature births rate (premature) are still on the rise, and the most important diseases suffered by the child’s premature (respiratory distress syndrome, septicemia, retinopathy, acute renal and pulmonary popular growth deficit) failure, so these births have become the primary and the main reason increase the proportion of morbidity and mortality among newborns on the world level.
Therefore, a correct diagnosis and appropriate treatment good for this disease associated with this category of birth of the most critical issues facing the field of newborn babies and that must be taken into account properly.
The innovative developments in scientific techniques that lead to progress in understanding the disease and in the diagnosis and treatment method, such as Genome Sciences, which has become the most important modern science and useful in all fields example: - the completion of the human genome in 2003, the project and the subsequent work of the Project (HapMap) International and through the study of variation DNA chain (De if any) provided the necessary technical resources to achieve progress in most fields of medicine, including the field of newborn babies.
from here, the proper integration appropriate for Science genome to this field of medicine gives great opportunities for progress in methods of diagnosis, care and treatment, and has been designed by well-genetic studies on the effect of variation of DNA chain (De if any) on the health and disease of the newborn allowed real opportunities and worthwhile to improve the diagnosis and treatment of neonatal patients and premature newborns impaired immune ways. We have characterized the genetic component of a number of diseases suffered by children in intensive care units for newborns.
The aim of this letter is to have been the work of a review scientific articles and books and scientific references that dealt with the study of the active role of the strong science genome in intensive care units for newborns and the study of the genetic component of months in the disease and to try to reduce the rate of these diseases occur and the proportion of the resulting deaths.
So it has recommended per message with some recommendations, such as: -
1. Increase the medical and scientific attention on the genome science and its role in the intensive care unit for newborns.
2. You must advise pediatricians to update their knowledge about the genome science and its role in the intensive care unit for newborns.
3. The Ministry of Health and other relevant institutions in Egypt to provide more financial support and encourage research on genomics and its role in the intensive care unit for newborns, to give further progress in this area and make it viable in the country.
Promote exchanges between the Egyptian universities and other prestigious universities and programs for the latest technology in research applications through the introduction of outside experts brought in this area