Newborn screening and early treatment of Mucopolysaccharidosis type I (MPS I) — a rare genetic disease — is now possible, thanks to breakthrough study by Mackay Memorial Hospital. MPS I is caused by a defect in the gene that disrupts the production of an enzyme called alpha-L-iduronidase (IDUA), which eventually leads to organ damage and death. The hospital’s pediatric genetics director, Lin Shuan-pei (林炫沛), said that babies with the disorder display no symptoms at all after birth, which is why early diagnosis is so important.
Infertility treatment (IVF) ,Rare Disease Treatment,Joint Replacement, Health Examination, MMHIMSC,Taipei ,Taiwan
Thursday, November 14, 2013
Rare genetic disorder can be detected early
張貼者:
Mackay International Medical Service Center
於
9:45 PM
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標籤international medical servise
Congenital Disease罕见疾病
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Mucopolysaccharidosis
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黏多醣症
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