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The National Society of Human Genetics - Egypt

The National Society of Human Genetics - Egypt. The human genetics activity started in the National Research Centre as a unit in 1966. As a department in 1977. Then became a Division with eight departments since 2003.

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The National Society of Human Genetics - Egypt

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  1. The National Society of Human Genetics - Egypt The human genetics activity started in the National Research Centre as a unit in 1966. As a department in 1977. Then became a Division with eight departments since 2003. Realizing the importance to promote Human Genetics as a science and to meet our patients social and ethical aspects, the National Society of Human Genetics- Egypt has been established in 2005.

  2. Objectives Increase of public awareness about the prevention and management of genetic diseases through the mass media and communications through newspapers, television& radio programs. Increase public knowledge about care & rehabilitation of genetically disabled through leaflets to be distributed to the public.

  3. Objectives Encouragement of students and recent graduates to join the activities of the society. Enhancement of national, regional and international networking and-co-operation for early   detection, prevention and management of genetic diseases which affect all systems and organs of the human body at the level of Egypt, Arab countries, Africa, Europe, USA…etc. At the executive committee meeting of the IFHGS, on November 3,2010,in Washington DC, USA, The National Society of Human Genetics Egypt was accepted as a corresponding member in the IFHGS. Thus becoming the first member in the Federation from Egypt and from the Arab world to be so honored . (http://www.ifhgs.org/)

  4. Activities •  Invited speakers for recent progress in genetic diseases • Joseph Gleason M.D, Ph.D. Head of Neurogenetics Laboratory. Neuroscience Department. University of California. “Recent approach in neurodevelopmental disorders”. 8/2/2006, 2007, 2008. • SaddafFarooqi M.D., Consultant technologist, Welcome Clinical Scientist, Cambridge University, UK. “Diagnosis and management of congenital leptin disorders in Obese Children”. 20/2/2006. • Olaf York, Head of Pediatric Endocrinology, Lubeck University, Germany. “Genetics of Intersex” 15/3/2006.

  5. Activities •  Invited speakers (continued): • WeemDorlin, Representative of Agilent Company for European Technology. “Sureprint microarraytechnology-a foundation for study of system genomics”. Agilent 2100 bioanalyser lab-on-a chip technology: endless possibilities for RNA/DNA and patients analysis”. 15/6/2006. • Elliott H. Sherr M.D., Ph.D. Department of Neurology, University of California, San Francisco. “Agenesis of corpus callosum: approaches to gene discovery and functional analysis”. 2/7/2006. • Albert Schinzel M.D. University & Zunich:A series of 7 lectures on chromosomal aberrations. April,   2003

  6. Projects Medical treatment of patients with osteogenesis imperfecta. Constructing a data base for genetic disorders in Egyptians. Towards the increase of public awareness about genetic diseases the society is publishing a series of booklets

  7. Treatment of OsteogenesisImperfecta

  8. conferences The first international conference of the society in conjunction with the African Society of Human Genetics was held in November 2007 in Cairo.

  9. conferences

  10. conferences The First International Conference of The Human Genetics and Genome  Research Division and National Society of Human GeneticsHuman Genetics and Genomics: Challenges For Proper Health November 8-10-2010

  11. Launching of Our Journal MEJMG Due to the need of Human Genetics Journal Reporting Genetic Problems in the Region, We initiated the Middle East Journal of Medical Genetics (MEJMG). We Established the International Editorial Board. We received articles for publication which are currently being reviewed in preparation for publication. The Journal has been welcomed by International Publishers but we have insufficient funds. We need your Help to achieve our goals!

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