Still, the pathogenic theory of schizophrenia runs counter to years of orthodox thinking that schizophrenia is a congenital, organic brain disorder.
这种解释精神分裂症的病原学说仍与多年来根深蒂固的主流学说相悖。主流观点是，精神分裂症是一种先天的器官性脑障碍。
Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.
先天性小眼球是一种先天发育异常性眼科疾病，遗传方式有常染色体显性遗传、常染色体隐性遗传和X连锁隐性遗传。
Chronic granulomatous disease (CGD) is a rare congenital disorder characterized by repeated bacterial and fungal infections.
慢性肉芽肿性疾病(CGD)是一种少见的先天性疾病，其特征为反复细菌和真菌感染。
Central cyanosis makes a congenital cardiac disorder highly likely.
中心型发绀提示先天性心脏病的可能性极高。
Question: If after an ultrasound examination, a pregnant woman finds out that her fetus has a congenital disorder, such as Down's Syndrome, is abortion allowed in this situation?
问：若是孕妇照超音波后，发现肚里的胎儿是畸形儿，如蒙古症之类的，请问可否因此堕胎吗？
The appearance of this disorder can include hypertelorism (widely-set eyes), down-slanting eyes, webbed neck, and other conditions, including congenital heart disease in half of those affected.
这种病症的表象可能包括器官距离过远（双目远离）、向下斜视、蹼状颈、以及其它状况，包括半数患有先天性心脏病。
Cleft palate: Fairly common congenital disorder in which a fissure forms in the roof of the mouth.
颚裂：一种常见的先天性疾病——胎龄两个月时颚板未能融合而遗留裂隙。
Question: Wouldn't it be very difficult for the parents to raise a child with a congenital disorder?
问：可是父母抚养这样的孩子，不是一辈子很辛苦吗？
Bart syndrome is a genetic disorder characterized by the association of congenital localized absence of skin, epidermolysis bullosa, lesions of the mouth mucosa, and dystrophic nails.
一种遗传疾病，以先天性局部皮肤缺损、大疱性表皮松解症、口腔粘膜病变、甲营养不良为特征。
Insufficient or poorly working myelin causes a number of diseases, including a rare and fatal congenital disorder called pediatric leukodystrophy that affects thousands of children.
髓磷脂不足或工作状态差可导致一系列疾病，包括影响几千个孩子的一种罕见与致命的遗传病：小儿脑白质营养不良。
Keratitis, ichthyosis, and deafness syndrome (KID syndrome) is a rare congenital disorder disease.
目的观察角膜炎、鱼鳞病、耳聋综合征的临床表现。
Congenital afibrinogenemia is a rare autosomal recessive disorder, characterized by the complete absence or extremely reduced level of fibrinogen.
遗传性无纤维蛋白原血症是一种由于纤维蛋白原基因缺陷所致常染色体隐性遗传病。
A similar, less severe, metabolic disorder is congenital lactase deficiency.
类似的，病症略轻为一点的代谢紊乱疾病是乳糖分解酶素缺乏症。
A similar, less severe, metabolic disorder is congenital lactase deficiency.
类似的，病症略轻为一点的代谢紊乱疾病是乳糖分解酶素缺乏症。
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