Reproduction & inbred genetic diseases is not rocket science!

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The battle between science and advanced medicine and obscurantism of tradition dating is a lost cause by that!
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Location of genes involved in neurological diseases in three consanguineous families Lebanese!
http://www.savoirs.essonne.fr/fileadmin/bds/MEDIA/les_technologies/information_communication/Telemedecine/telemedecine_cerveau.jpg (http://translate.googleusercontent.com/translate_c?hl=fr&langpair=fr%7Cen&rurl=translate.google.fr&u=http://www.savoirs.essonne.fr/&usg=ALkJrhitt_8HTUOs4p1ifcVurrqu_Z2I-g)
http://www.neuromuscular-lamin-inserm.fr/Site%20Fr/images/libanvign.jpg (http://translate.googleusercontent.com/translate_c?hl=fr&langpair=fr%7Cen&rurl=translate.google.fr&u=http://javascript%253cb%253e%253c/b%253E:afficheMaxi%28%27images/liban.jpg%27%29&usg=ALkJrhg55UZoI9UshsCDasCY2lPwaInO7w) It was studied three consanguineous families Lebanese with hereditary neurological diseases transmitted in an autosomal recessive.
http://www.mcps.k12.md.us/SCHOOLS/WJHS/MEDIACTR/scipathfinder/genetics/img/hands_up.gif
The three conditions are: a form of demyelinating disease Charcot-Marie-Tooth disease autosomal recessive (CMT4F), and two new forms of non-progressive congenital ataxia autosomal recessive ataxia of Norman type, associated a small and a new ataxic syndrome associated with mental retardation, optic atrophy and ultra structural abnormalities of the skin, which we called CAMOS.
By Isidore AYA TONGA founder www.seleo.fr (http://translate.googleusercontent.com/translate_c?hl=fr&langpair=fr%7Cen&rurl=translate.google.fr&u=http://www.seleo.fr/&usg=ALkJrhivTQi21-T5MesSs0TfiZf6At9HbA) & de www.seleo.biz (http://translate.googleusercontent.com/translate_c?hl=fr&langpair=fr%7Cen&rurl=translate.google.fr&u=http://www.seleo.biz/&usg=ALkJrhjhgtd3ZvddE2JxEqOQ9ApIIxLYng) ; your ambassador total digital extension of scientific culture!

[admin]

France, consanguineous marriages, genetic diseases & Social Security!
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Stop complaining to your nonsense! Some suffer more lasting & ...But who? ... Children genetic diseases because of your ignorance of inbreeding and all its implications medico!
Why is it prohibited by the Act (sections 161, 162, 163, 164, 366 and 342-7 of the Civil Code) to marry brothers and sisters, his uncle and his niece?
The ban certainly taken over by religious or "moral" is actually based on an observation: the children of consanguineous unions (that is, between relatives) have an increased risk of certain diseases, which are genetic diseases.
http://www.mariage-fr.net/html/images/musulman.jpg
Spring 1998: "Mohammed married his first cousin, Zohra and had five children. Two normal children happily" insha'Allah "and three genetic diseases, unfortunately."
But whose fault? ... A inbreeding. ... It's not rocket
But how to explain it? ... Science ... Molecular biology, genetics formal and Reproductive Medicine can only be explained as a breeze!
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Social Security continues to dig its hole by spending huge amounts of money to support medical & hospital for sick children from these genetically consanguineous marriages.
But why does the law does not preclude further and it not these marriages between cousins?

Why Inbreeding increases the risk of developing certain genetic diseases?
This is the inheritance of mutations that can explain this phenomenon.
In a large population, there are many rare recessive alleles.
To the extent that unions are random and the number of people is high, the risk that two healthy people carry the same recessive mutation occur is low.
For each known recessive disease, the risk of birth of an affected individual is the frequency of the disease in the population.
Taking the example of cystic fibrosis, a couple has a risk of giving birth to a child with 0.04%, which corresponds to the frequency of the disease (1 in 2500).
This reflects the fact that 1 in 25 in the healthy population are carriers of a mutation causing the disease in the heterozygous state.
http://www.savoirs.essonne.fr/fileadmin/bds/MEDIA/le_patrimoine/histoire_des_sciences/Gregor-Mendel/Mendel_genome.jpg
However, within the same family, the probability of finding a mutation in the heterozygous state in individuals belonging to different generations and branches is increased. In fact, these anomalies are somehow "concentrated" in the family because of their inheritance.
The risk for a couple from the same family to give birth to a child homozygous for one (or sometimes more) mutation (s) Family (s) is therefore higher than in the general population.
This is why genetic diseases are more common in children from a consanguineous union.
The more the relationship is closer, that risk is high.
To take the example of cystic fibrosis, the union between first cousins ​​increases the risk of giving birth to a sick child: the risk is 0.0412, that is to say, it is multiplied by more than 100.

For more info in the image, click here: # http://www.seleo.fr/forum/vbtube_sho...beid=160 watch (http://translate.googleusercontent.com/translate_c?hl=fr&langpair=fr%7Cen&rurl=translate.google.fr&u=http://www.seleo.fr/forum/vbtube_show.php%3Ftubeid%3D160&usg=ALkJrhgk3DGSkgAvHhHuSAUyC-PUId04bQ#watch)

By Isidore AYA TONGA founder www.seleo.fr (http://translate.googleusercontent.com/translate_c?hl=fr&langpair=fr%7Cen&rurl=translate.google.fr&u=http://www.seleo.fr/&usg=ALkJrhivTQi21-T5MesSs0TfiZf6At9HbA) & de www.seleo.biz (http://translate.googleusercontent.com/translate_c?hl=fr&langpair=fr%7Cen&rurl=translate.google.fr&u=http://www.seleo.biz/&usg=ALkJrhjhgtd3ZvddE2JxEqOQ9ApIIxLYng) !