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珀金埃爾默醫(yī)學診斷產(chǎn)品（上海）有限公司
珀金埃爾默醫(yī)學診斷產(chǎn)品（上海）有限公司
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更新時間：2022-10-12 13:20:16瀏覽次數(shù)：68次
聯(lián)系我時，請告知來自 環(huán)保在線Galactosemia is an inherited disorder caused by a deficiency of one of three enzymes responsible for the metabolism of α-D-galactose. The most common form of the disease, classic galactosemia is cause......
If not diagnosed and treated within the newborn period, it can lead to diarrhea, dehydration, jaundice, hepatic failure, hypoglycemia, cataracts, developmental retardation, and death within a few weeks. Treatment of the disease consists of withdrawal of all foods containing lactose and galactose from the diet.
GSP Neonatal GALT - the first automated GALT assay
The GSP Neonatal GALT assay is used as an aid in screening newborns for classic galactosemia caused by GALT deficiency using the GSP™ instrument.
| 檢測技術(shù) | Enzymatic |
|---|---|
| 校準標準 | Yes |
| 檢測方法 | Enzymatic |
| 疾病 | Galactosemia |
| 產(chǎn)品品牌名稱 | GSP® |
| 樣品類型 | Dried blood spots |
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