Jacobson Syndrome: An Overview

Other names of Jacobson's syndrome: 11 q terminal deletion disorder 11 q deficiency Jacobson thrombocytopenia cause of JBS disorder: Jacobson syndrome occurs when the genetic material of chromosome 11 is lost. There is a deletion at the end of long arm (q) of chromosome 11. Affected chromosome: chromosome 11 - deletion at the end of long arm (q). Is there a prenatal diagnosis? Many children are diagnosed with Jacobson syndrome after birth, but cell analysis can be used for prenatal testing.

Polycystic ovary syndrome (PCOS) affects women and is a causative disease that causes hormonal imbalance in women (Polycystic Ovary Syndrome, 2012). Polycystic ovary syndrome (PCOS) - According to the summary of the topic (2005-2012), "It can cause problems in your menstrual cycle and make it difficult to get pregnant. As time goes on, diabetes and It may cause serious health problems such as heart disease (paragraph 1) PCOS is very common, affecting 1 out of 15 women (polycystic ovary syndrome (PCOS ) - topic overview, 2005 - 2012)

In the previous article, we briefly outlined the Turner syndrome first and then focused on the cardiac complications usually revealed by the symptoms. So what does genetics have on Turner's syndrome and what do we understand about it? Turner's syndrome can be described from another perspective - as a childhood, cardiovascular or female condition etc. However, it is often described as a genetic disorder or condition. Like other genetic conditions, Turner syndrome occurs due to the amount of genetic information stored in each cell. In the case of Turner's syndrome, women are partially or completely lacking genetic material in their X chromosomes. However, unlike most other hereditary diseases, Turner's syndrome is sporadic in most cases.

Hereditary diseases include Turner's syndrome, Down's syndrome, and achondroplasia. Turner syndrome means that health problems are caused by excessive chromosomes, too little, or confusion. This is a common genetic disorder that occurs only in girls. It does not cause bad growth, late or puberty. Turner's syndrome occurred in one out of 2,500 women. It is caused by the missing X chromosome. Down syndrome is another common genetic disorder that causes poor growth and short stature. It comes from extra chromosome 21. Chondrogenic dysfunction is the most common hereditary bone disease. Children's arms and legs may shorten. It also leads to big heads and other functions

Down syndrome is an increasingly common disease in the United States. This is an inherited disorder caused by extra chromosome 21. One in 800 births is Down Syndrome (National Down Syndrome Association). Down syndrome is the most common form of identifiable delay (Ludman and Wynbrandt, p. 23) and genetic disease (National Down Syndrome Association). Down syndrome was initially thought to be a disease by John Langdon Down in 1866 and is called "father" of Down syndrome with the same name as Down. The original name of Down's syndrome was "a fool of Mongolia" due to the inclination of the eyes and a flat face (National Down Syndrome Association). He thinks this is a counterattack against Mongolian ancestors, but that word is now considered to be outdated and aggressive. But centuries ago, the characteristics of Down's syndrome were discovered in art, literature and science (National Down Syndrome Association).