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- We understand ugliness and fatness are genetic disorder. 我们把丑陋,肥胖看作基因错乱。
- Two of his grandchildren developed a rare genetic disorder and one died. 他的两个孙儿得了一种罕见的遗传疾病，其中一个已经离开人世。
- Two of his grandchildren developed a rare genetic disorder, and one died. 他的两个孙儿得了一种罕见的遗传疾病，其中一个已经离开人世。
- The transplant recipients will be children who suffer from a rare, fatal genetic disorder. 移植对象为患罕见的,致命的遗传疾病的儿童。
- Among the Ashkenazi Jewish population, Gaucher disease is the most common genetic disorder, with an incidence of approximately 1 in 450 persons. 在德系犹太人中，戈谢病是最普遍的基因突变疾病，大约为1/450。
- Congenital adrenal hyperplasia is a genetic disorder transmitted by autosomal recessive pattern. 摘要先天性肾上腺增生症是一种自体隐性遗传病。
- Incontinentia Pigmenti (IP) is a genetic disorder that affects the skin, hair, teeth, and nails. 什么是'色素失禁症-继承多系统疾病的影响皮肤毛发的牙齿和指甲'?
- Paula, who suffered from the genetic disorder porphyria, lapsed into a coma in 1991 and died in 1992. 葆拉由于受到遗传性的代谢紊乱的折磨，在1991年进入了昏迷麻木的状态，1992年死亡。
- Narcolepsy affects about 1 in 2,000 people, and is thought to be a genetic disorder. 两千个人中就会有一个人得嗜睡症，并且通常认为嗜睡症是一种遗传疾病。
- Dentin dysplasia is a genetic disorder of teeth, commonly exhibiting an autosomal dominant inheritance. 什麽是'牙本质发育异常-牙本质发育异常'?
- Crook, 61, suffers from Gardner's syndrome, a genetic disorder that can cause multiple polyps and desmoid tumors. 硬纤维瘤是一种具有侵袭性的软组织肿瘤，能浸润破坏周围的健康组织和器官。虽然它不会转移，但是也会威胁生命。
- Normally inoled in the response to stress and repair of DNA, ATM is mutated in the rare genetic disorder ataxia-telangiectasia (AT). ATM正常情况下参与应激反应和DNA修复，在罕见的遗传性紊乱疾病--共济失调性毛细血管扩张症（AT）中，ATM发生变异。
- Human embryo preimplantation genetic diagnosis (PGD) for sure can solve some problems who have genetic disorder or disease. 人类胚胎着床前遗传学诊断（PGD）能解决诸多有关遗传学异常或疾病的问题。
- Nevoid basal cell carcinoma syndrome is a rare autosomal dominant genetic disorder characterized by developmental abnormalities and tumorigenesis. 痣样基底细胞癌综合征是一种罕见的常染色体显性遗传病,以发育异常和肿瘤发生为主要临床特征。
- TSC is a genetic disorder that causes benign tumors to form in many different organs, primarily in the brain, eyes, heart, kidney, skin and lungs. TSC是一种遗传性疾病，导致良性肿瘤的形成，在许多不同的器官，主要是在脑部，眼睛，心脏，肾脏，皮肤和肺部。
- Reconstructing the face of a person who was in an accident, has suffered from cancer, or has a genetic disorder was once the subject of science fiction. 重塑因事故、罹患癌症或遗传疾病造成缺陷的面孔(一度成为科幻小说的主题)。
- Background: Fibrodysplasia ossificans progressia is a rare genetic disorder of ectopic skeletogenesis associated with dysregulation of bone morphogenetic protein (BMP) signaling. 背景：进行性骨化性纤维发育不良是一种表现为异位骨化和BMP信号传导失调的少见的遗传性疾病。
- Tuberous sclerosis is a rare genetic disorder characterized by a triad of signs: seizures, mental retardation, and small benign facial skin tumors (angiofibromas). 什么是'结节性硬化症-遗传性疾病导致神经体系和皮肤问题'?
- Treacher Collins syndrome (also known as Franceschetti-Zwahlen-Klein syndrome or mandibulofacial dysostosis) is a rare genetic disorder characterized by craniofacial deformities. 什麽是'特雷彻-柯林斯综合徵-遗传疾病造成面部和头颅畸形'?
- Congenital hyperinsulinism (CH) is a genetic disorder characterized by inadequate suppression of insulin secretion in the presence of recurrent hypoglycemia. 先天性高胰岛素血症（CH）是一种遗传性疾病，其特点是胰岛素分泌抑制不足，经常发生低血糖症。
