i（17q）探针

i（17q）探针

 广州健仑生物科技​有限公司 

本司长期供应尼古丁（可替宁）检测试剂盒，其主要品牌包括美国NovaBios、广州健仑、广州创仑等进口产品，国产产品，试剂盒的实验方法是胶体金方法。

我司还有很多荧光原位杂交系列检测试剂盒以及各种FISH基因探针和染色体探针等，。

i（17q）探针

   本试剂盒主要用于i（17q）的检测，17q等臂染色体是在肿瘤中zui常见的等臂染色体，预后极差。
本试剂盒仅供科研使用。

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【公司名称】 广州健仑生物科技有限公司
【】    杨永汉 

【】
【腾讯 】
【公司地址】 广州清华科技园创新基地番禺石楼镇创启路63号二期2幢101-3室

【企业文化宣传】

每年2月的zui后一天是世界罕见病日。记者从广东省医学会罕见病学分会了解到，目前范围内已确认的罕见病种占人类疾病的10%左右，总数有6000~7000种，多数是先天性因素引起的“疑难杂症”。

广州市妇女儿童医疗中心儿童内分泌科刘丽教授介绍，罕见病70%~80%能找到基因上的问题，表现多种多样，有的是神经系统症状，有的是肝脾系统症状，顽固性贫血也可能是罕见病引起。如果是有家庭聚集性、诊断不明确、治疗效果不明显等“与众不同”的病，就要警惕是罕见病的可能。

专家提醒，假如家有疑似患有罕见病的孩子想再生育一个健康的孩子，在再次生育前，首先应该明确诊断孩子患的是什么疾病，在备孕前接受遗传咨询，了解再次生育同样疾病孩子的风险、是否适合再次生育。再次怀孕后，应该在怀孕15周以内及早进行产前诊断，看看胎儿是否患有同样疾病并进行处理。对于自身患有罕见病，希望生个健康的宝宝的人群来说，同样可以通过遗传咨询、产前诊断来中断遗传。

刘丽介绍，由于不同罕见病有多种症状，患者分散在不同科室，一般医生每年碰到的某种罕见病患者非常有限，要让所有相关医生都熟练掌握各种罕见病的诊断、治疗并不现实，如今省医学会罕见病学分会正在组建罕见病医联体，由广州市内部分大医院及粤北、粤西、粤东等地市县医院组成，通过网络对基层医疗接收到的疑难病例进行会诊，远程指导当地医生为患者做相应检查，将可疑病例转到大医院进行集中治疗。在大医院接受治疗后病情稳定的患者，可以下转回基层医院，并由大医院医生通过网络对当地医生指导后续治疗。

The last day of February is the rare day of the world. Reporters from the Guangdong Provincial Medical Association rare disease branch learned that rare diseases worldwide confirmed human diseases accounted for about 10%, the total number of 6000~7000, mostly caused by congenital factors Difficult miscellaneous diseases "".

Professor Liu Li, a child Department of endocrinology in Guangzhou women's and children's Medical Center, introduced rare diseases. 70%~80% can find genetic problems. There are various manifestations. Some are neurological symptoms. Some are symptoms of liver and spleen system. Refractory anemia may also be caused by rare diseases. If there is a family aggregation, the diagnosis is not clear, the treatment effect is not obvious and so on "different" disease, we should be alert to the possibility of rare diseases.

The expert reminds, if there are suspected of suffering from a rare disease of children want to give birth to a healthy child, again before birth, first of all should be clear what is the diagnosis of children suffering from disease, in the preparation of pregnancy received genetic counseling, again have the same disease risk, understand whether it is suitable for child birth again. After another pregnancy, it should be carried out early in the 15 weeks of pregnancy for prenatal diagnosis, to see if the fetus is suffering from the same disease and to be treated. Genetic counseling and prenatal diagnosis can also be used for people who have a rare disease and want to have a healthy baby.

Liu Li, due to a variety of different symptoms of rare diseases, patients scattered in different departments, general practitioners of a rare disease patients met every year is very limited, to all relevant doctors are skilled in diagnosis, all kinds of rare disease treatment is not realistic, now the Medical Association of rare diseases branch is the formation of rare disease conjoined by Guangzhou city hospital and divided northern and Western and eastern counties such as hospitals, through consultation of difficult cases received primary care network, remote guidance of local doctors do the corresponding examination for patients suspected cases will be transferred to a big hospital for centralized treatment. Patients with stable disease after receiving treatment in large hospitals can be transferred back to the basic level hospitals, and the doctors in large hospitals can guide the follow-up treatment for local doctors through the Internet.