婴儿遗传性多囊肾后天畸形怙恃诉病院未告诉 法院判补偿12万(国外英文资料).docVIP

婴儿遗传性多囊肾先天畸形父母诉医院未告知 法院判赔偿12万(国外英文资料) The parents of the genetic polycystic kidney disease were not told the court awarded 120,000 yuan In todays society, the incidence of nephropathy is higher and higher, especially in infants, with a 50% genetic rate. In one of the cases Ive seen today, theres a lawsuit over the genetic polycystic kidney in babies. Morning paper dispatch (wong pregnancy in pinggu a hospital for a pregnancy test, seven examination all showed normal fetus, but there are no left hand was told after the child is born with congenital polycystic kidney. Ms. Wang believes that hospital and inform obligation, a duty of care not to implement it violated their right to know and reproductive options, so the appeal claims 480000 yuan. A reporter recently learned that the pinggu court sentenced the hospital compensation wang more than 120000 yuan. Relative to kidney disease, everyone for polycystic kidney should know much, polycystic kidney disease is a kind of what kind of disease, by now Beijing cluster technology limited kidney disease hospital experts explain for everybody polycystic kidney. Polycystic kidney disease is a common hereditary kidney disease, main show is bilateral renal cyst of multiple sizes, cyst progressive increase, eventually damage the kidney structure and function, leads to end-stage renal failure. Why is this disease? What is the cause of the polycystic kidney? This disease is autosomal dominant inheritance, according to its genetic law, the generation of disease, the incidence of male and female disease is equal. Parents have a 50 percent chance of developing a disease. But about 40 per cent of patients have no family, and may be caused by a mutation in their own genes. The ADPKD mutated gene is known to have two genes and is known as PKD1 and PKD2 respectively. PKD1 is located in the short wall of chromosome 16 (16p13. 3). The length of the gene is 52kb, with 46 exons, and the mRNA is 14kb. PKD2 is located on the 4th chromosome arm