迪格夫-梅尔基奥-克劳森综合征与腹腔疾病:一种罕见的实体
Ali S Alquraishi1, Sami E Abdelmogeit2, Khalid Asiri3
1Pediatrics, Endocrinology Unit, Armed Forces Hospital Southern Region, Khamis Mushait, SAU.
Cureus
|March 17, 2025
概括
迪格维-梅尔基奥-克劳森综合征是一种罕见的遗传疾病,在一名沙特男孩身上发现了一种新的DYM基因突变. 这一案例突显了与乳病的异常共发生.
科学领域:
- 遗传学 是一个遗传学.
- 儿科 儿科 儿科
- 罕见疾病 罕见疾病
背景情况:
- 迪格维-梅尔基奥-克劳森综合征 (DMC) 是一种由DYM基因突变引起的自体骨发育不良,呈现出发育迟缓,骨变形和粗的面部特征.
- DMC综合征的遗传基础涉及DYM基因的致病突变,导致具有特征的骨异常.
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