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brother all the family who died in infancy, 30-year-old Liu Sichuan has experienced too many childhood life to death. When the 8-month-old son also died, the The Children's Hospital of Chongqing Medical University genetic diagnosis, the family suffers from a rare primary immunodeficiency disease, due to mutations in children with recurrent infections lead to death.
6 men all died
day before yesterday, Sichuan Daxian Liu uneasy with a 4-month-old son, Fufu (a pseudonym) to review the Children's Hospital of Chongqing Medical University. After inspection, all the indicators Fufu normal body, a result that she burst into tears.
Liu from Sichuan Daxian Xuanhan Nong Village, recalled the past many life and death, she said he did feel like a nightmare. Ms Lau said that she is the boss at home, there is still a sister. But apart from them two sisters, the mother gave birth to five brothers, but each brother in infancy, recurrent colds and other symptoms occur under the die, a younger brother to live up to only live for seven months. Their home,
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2007 years, the family's At first thought it was only a cold, fever, did not think the stars are endless, take medicine, transfusion have no effect. Fever almost every day, should eat antipyretics. 8 months until the dying stars, the family members sent him to Children's Hospital of Chongqing, but because of late, the stars rapidly died.
rare immune disease causing trouble
's about listening to Ms. Liu, the Children's Hospital experts was shocked, why a family of men in infancy were able to escape the claws of death? Children's Hospital immediately sampling the stars,
tory burch online, and then genetic testing and diagnosis, and ultimately found that the stars suffer from X linked chronic granulomatous disease, that neutrophil oxidative function in children with deficiency, is an immune deficiency disease. Carry genes that cause women give birth to the baby, the baby half the risk of carrying disease genes, half of the chance of the baby is sick.
Immunology, Children's Hospital, according to Professor Jiang Liping introduced, the disease is a rare immunodeficiency disease, only 50 cases of domestic children about the stars is the second hospital patients by genetic diagnosis. Neutrophils could kill bacteria, fungi, etc., but appeared after the oxidation of functional defects,
tory burch flats, it is vulnerable to bacteria and fungi, a little cold will soon develop into pneumonia, and basically no cure for cure, the only way is the same as leukemia, stem cell transplantation can be expected by completely cured. However,
tory burch sale, due to difficulties in diagnosis of the disease, most children with a disease, not yet confirmed the cause to have died.
give birth to healthy baby monitor in advance
hospital through genetic diagnosis, Ms. Liu found the body carry disease genes. Thus, Sharon was heartbroken not to have children, they were unwanted pregnancies in the last year, but also boys.
experts to immediately remove the fetus from her body amniotic fluid cells, and analyzed for genetic testing. Fortunately, the detection of disease genes found not carrying the baby, according to doctor's told and monitoring, Liu birth to baby boy at the end of last year. The day before yesterday, has 4-month-old boy once again came to Children's Hospital review, the results show everything is normal.
the hospital to remind parents of immunization experts, Professor Jiang Liping,
tory burch shoes, for children with recurrent infections immunological screening must be done, do the relevant disease gene diagnosis, specifically members of the family carriage. To have the immune deficiency disease in female carriers of the fetus,
tory burch bags, we must do a good job early prenatal counseling and genetic testing. Reporter Likui