Edwards ' also known syndrome under the name of 18 trisomy. Edwards ' genetic chromosomal disorder rare of syndrome occurs when a child is constant with three copies of chromosome 18, rather than the two usual ones. Trisomy 18 is a relatively common syndrome roughly affecting 1 out of 3.000 births of phase.

It assigns people of all the cultural mediums and becomes more probable with the increase in the maternal age. The syndrome is caused by the presence of an additional material of chromosome 18. The additional material interferes the normal development. Trisomy 18 severely affects all the systems of body of the body.

Edwards syndrome causes leading physical abnormalities and serious psychological retardation, and really few children afflicted with this disease endure beyond a year. Women old than their earlier thirties have a greater danger of conceiving a kid with trisomy 18, but it can happen in younger women. Surviving children with Edwards' syndrome have marked developmental and motor delays.

The symptoms can include the mental delayed-action and the delayed development (100% of the individuals), the high tonality of muscle, the physical seizures, and malformations such as defects of brain. The majority of the children supported with Edwards ' syndrome seem weak and fragile, and they are often of insufficient weight. The head is exceptionally small and the back of the head is ahead. The ears are badly formed and low-place, and stops it and the jaw are small.

Edwards syndrome causes leading physical abnormalities and serious psychological retardation, and really few children afflicted with this disease endure beyond a year. Women old than their earlier thirties have a greater danger of conceiving a kid with trisomy 18, but it can happen in younger women. Surviving children with Edwards' syndrome have marked developmental and motor delays.

Their verbal communication is severely impaired, and is limited to a few single words at best, but they are mostly aware of their environment and are able to communicate some of their needs non-verbally.

Single-gene defects – More often than not, single gene defects are inherited. Phenylketonuria, for instance, is a condition which can be inherited as caused by the malfunction of the PAH enzyme. It breaks down the body's amino acid phenylalanine. Single gene defects are prevalent in some ethnic groups. Sickle-cell anemia is common among Indians and Africans. Tay-Sachs, on the other hand, which is said to be caused by lack of protein hexosaminidase, is common among Jews.

Single-gene defects – More often than not, single gene defects are inherited. Phenylketonuria, for instance, is a condition which can be inherited as caused by the malfunction of the PAH enzyme. It breaks down the body's amino acid phenylalanine. Single gene defects are prevalent in some ethnic groups. Sickle-cell anemia is common among Indians and Africans.

The ultrasound started out great, baby was sleeping so we got some good shots at first, then he woke up, curled into a ball and hid below my pelvic bone. The tech seemed obsessed with getting good pictures of his little feet (which are cute, but really, do we need to spend 15 minutes on this?)

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