兒童稀有病及發育遲緩測試

測試由韓國第一大藥廠 (GC Pharma)附屬DNA 化驗機構 (GC Genome)提供，只需七天，可以讓你更深入了解嬰兒未來發展的需要，及早知道，可以作出更好的安排及發展需要!

總共測試91種基因，包括但不限於 Prader-Willi/Angelman syndrome (天使症候群), Cat eye syndrome (貓眼綜合徵), Turner syndrome (透納氏症), Rieger syndrome, Cri-du-chat syndrome, Sotossyndrome, Grieg syndrome, Williams syndrome, Currarinosyndrome, Langer-giedionsyndrome, Kleefstrasyndrome, DiGeorgesyndrome, Potocki-Shaffer syndrome, Jacobsen syndrome, Pallister-Killian syndrome, Patausyndrome, , Smith-Magenissyndromem, Potocki-Lupskisyndrome, Miller-Diekersyndrome, Koolen-de Vriessyndrome, Edwards syndrome , Alagille’ssyndromeDiGeorgesyndrome, Phelan-McDermidsyndrome, Glycerol kinase deficiency, Nance-Horan syndrome, allmann’ssyndrome, Leri-Weill syndrome, Pelizaeus-Merzbacher syndrome, Klinefelter’s syndrome….