 | 2022/9/21 α-thalassemia | |  陳明醫師與遺傳諮詢中心團隊成員你好 我目前懷孕18周，先生具有地中海型貧血遺傳，日前接獲羊水晶片報告檢查分析結果為：One copy of deletion in chromosome 16p13.3 was found. The deletion spans about 15.5 Kb and contains 4 genes (including HBA1 and HBA2). Since the deletion is associated with α-thalassemia, genetic counseling is recommended.查了網路上相關資訊只知甲型地中海型貧血可分輕、中、重度，想請問依這報告可得知其嚴重度嗎？ 所謂帶原者是否指：帶有基因但不發病嗎？這會影響寶寶嗎? 萬分感謝貴團隊的回答 |  小*子 |
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