i（17q）探針

 廣州健侖生物科技?有限公司 

本司長(zhǎng)期供應(yīng)尼古?。商鎸帲z測(cè)試劑盒，其主要品牌包括美國(guó)NovaBios、廣州健侖、廣州創(chuàng)侖等進(jìn)口產(chǎn)品，國(guó)產(chǎn)產(chǎn)品，試劑盒的實(shí)驗(yàn)方法是膠體金方法。

我司還有很多熒光原位雜交系列檢測(cè)試劑盒以及各種FISH基因探針和染色體探針等，。

i（17q）探針

   本試劑盒主要用于i（17q）的檢測(cè)，17q等臂染色體是在腫瘤中zui常見(jiàn)的等臂染色體，預(yù)后極差。
本試劑盒僅供科研使用。

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二維碼掃一掃

【公司名稱(chēng)】 廣州健侖生物科技有限公司
【】    楊永漢 

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【騰訊 】
【公司地址】 廣州清華科技園創(chuàng)新基地番禺石樓鎮(zhèn)創(chuàng)啟路63號(hào)二期2幢101-3室

【企業(yè)文化宣傳】

每年2月的zui后一天是世界罕見(jiàn)病日。記者從廣東省醫(yī)學(xué)會(huì)罕見(jiàn)病學(xué)分會(huì)了解到，目前范圍內(nèi)已確認(rèn)的罕見(jiàn)病種占人類(lèi)疾病的10%左右，總數(shù)有6000~7000種，多數(shù)是先天性因素引起的“疑難雜癥”。

廣州市婦女兒童醫(yī)療中心兒童內(nèi)分泌科劉麗教授介紹，罕見(jiàn)病70%~80%能找到基因上的問(wèn)題，表現(xiàn)多種多樣，有的是神經(jīng)系統(tǒng)癥狀，有的是肝脾系統(tǒng)癥狀，頑固性貧血也可能是罕見(jiàn)病引起。如果是有家庭聚集性、診斷不明確、治療效果不明顯等“與眾不同”的病，就要警惕是罕見(jiàn)病的可能。

專(zhuān)家提醒，假如家有疑似患有罕見(jiàn)病的孩子想再生育一個(gè)健康的孩子，在再次生育前，首先應(yīng)該明確診斷孩子患的是什么疾病，在備孕前接受遺傳咨詢(xún)，了解再次生育同樣疾病孩子的風(fēng)險(xiǎn)、是否適合再次生育。再次懷孕后，應(yīng)該在懷孕15周以?xún)?nèi)及早進(jìn)行產(chǎn)前診斷，看看胎兒是否患有同樣疾病并進(jìn)行處理。對(duì)于自身患有罕見(jiàn)病，希望生個(gè)健康的寶寶的人群來(lái)說(shuō)，同樣可以通過(guò)遺傳咨詢(xún)、產(chǎn)前診斷來(lái)中斷遺傳。

劉麗介紹，由于不同罕見(jiàn)病有多種癥狀，患者分散在不同科室，一般醫(yī)生每年碰到的某種罕見(jiàn)病患者非常有限，要讓所有相關(guān)醫(yī)生都熟練掌握各種罕見(jiàn)病的診斷、治療并不現(xiàn)實(shí)，如今省醫(yī)學(xué)會(huì)罕見(jiàn)病學(xué)分會(huì)正在組建罕見(jiàn)病醫(yī)聯(lián)體，由廣州市內(nèi)部分大醫(yī)院及粵北、粵西、粵東等地市縣醫(yī)院組成，通過(guò)網(wǎng)絡(luò)對(duì)基層醫(yī)療接收到的疑難病例進(jìn)行會(huì)診，遠(yuǎn)程指導(dǎo)當(dāng)?shù)蒯t(yī)生為患者做相應(yīng)檢查，將可疑病例轉(zhuǎn)到大醫(yī)院進(jìn)行集中治療。在大醫(yī)院接受治療后病情穩(wěn)定的患者，可以下轉(zhuǎn)回基層醫(yī)院，并由大醫(yī)院醫(yī)生通過(guò)網(wǎng)絡(luò)對(duì)當(dāng)?shù)蒯t(yī)生指導(dǎo)后續(xù)治療。

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.