Through the past decade, a lot of syndromes have been discovered by different Scientists and some of them may be deadly such as meckel syndrome. (MGS) is a deadly and genetic disease caused by disorder in the genes and parents have a high potential to transfer it to their children. In fact, a study discovered using data from over one hundred and fifty cases of Meckel-Gruber syndrome, as accessed through the European Surveillance of Congenital Anomalies (EUROCAT) network, found the prevalence of various characteristics of this disease.(1) Also, people should know more about the back ground information, symptoms and how to diagnose (MGS).
The first reports of Meckel-Gruber syndrome were published in 1822 by Johann Friedrich Meckel. G.B. Gruber also published reports of patients with Meckel-Gruber syndrome in 1934. Meckel syndrome, also known as Meckel-Gruber syndrome, is a severe pleiotropic autosomal recessive developmental disorder caused by dysfunction of primary cilia during early embryogenesis. In addition, it has discovered that there is more than one gene can cause the disease and which genes on chromosome 8, 11 and 17. And it is a rare disease and the different incidence of this disease around the world at a rate of 1 to 1 …show more content…
The proper way to diagnose the disease during pregnancy is ultraviolet sound taken in the second trimester of pregnancy, "after ten weeks" because it would be easy to see hernia in the head as noted on the overall increase in the size and polycystic although the lack of liquid Caminos make the picture is not clear and if found liquid Caminos well radiologist may be able to detect an increase in the number of fingers. While helping magnetic radiation specialist along with ultraviolet voice in the detection of defects in the fetus even better with grandparents and a few in the liquid Caminos also describes the overall size and reveal the hernia is located in the
The first reports of Meckel-Gruber syndrome were published in 1822 by Johann Friedrich Meckel. G.B. Gruber also published reports of patients with Meckel-Gruber syndrome in 1934. Meckel syndrome, also known as Meckel-Gruber syndrome, is a severe pleiotropic autosomal recessive developmental disorder caused by dysfunction of primary cilia during early embryogenesis. In addition, it has discovered that there is more than one gene can cause the disease and which genes on chromosome 8, 11 and 17. And it is a rare disease and the different incidence of this disease around the world at a rate of 1 to 1 …show more content…
The proper way to diagnose the disease during pregnancy is ultraviolet sound taken in the second trimester of pregnancy, "after ten weeks" because it would be easy to see hernia in the head as noted on the overall increase in the size and polycystic although the lack of liquid Caminos make the picture is not clear and if found liquid Caminos well radiologist may be able to detect an increase in the number of fingers. While helping magnetic radiation specialist along with ultraviolet voice in the detection of defects in the fetus even better with grandparents and a few in the liquid Caminos also describes the overall size and reveal the hernia is located in the