融合功能发育不全是间歇性外斜视发病机制的主要因素。
The unsoundness growth of fusion function was the major pathogenetic factor in intermittent exotropia.
目的：探讨影像技术对孤立性右心室发育不全的诊断价值。
Objective: To investigate the value of diagnostic imaging for isolated right ventricular hypoplasia.
本病需与后颅窝蛛网膜囊肿、囊性新生物和变异的巨大枕大池以及重度小脑发育不全鉴别。
This disease should be differentiated from variation of the large cisterna magna arachnoid cyst of the posterior forssa cystic neoplasm and severe hypoplasia of the cerebellum.
早产儿易于发生呼吸问题、器官发育不全、感染和脑性麻痹。
Premature babies are vulnerable to breathing problems, underdeveloped organs, infections and cerebral palsy.
局灶性真皮发育不全综合征是一种罕见的遗传性皮肤病，其特征是进行性皮肤缺失，引起真皮发育不全，出现线状皮损，真皮层可见脂肪组织。
Focal dermal hypoplasia is a rare genodermatosis characterized by developmental defects of the skin, resulting in widespread linear lesions of dermal hypoplasia with adipose tissue in the dermis.
心律不整性右心室发育不全是一种少见的疾病，但是也是造成轻人猝死的主要原因之一。
Arrhythmogenic right ventricular dysplasia is a rare disease that sometimes leads to sudden death in young people.
目的：研究少汗性外胚叶发育不全引起先天缺牙的ED1基因突变。
Objective: To detect ED1 gene mutation in three hypohidrotic ectodermal dysplasia (HED) nuclear families.
它曾被报告与淋巴母细胞转变相关的急性骨髓性白血病、骨髓增生性疾病、脊髓发育不全症等等，甚至于那些不具已知的血液学异常相关的病人们身上。
It has been reported in association with acute myeloid leukemia, myeloproliferative disorders, and myelodysplasia in blast transformation, as well as in patients with no known hematological disorders.
它是一种异质性条件界定的任何视神经发育不全，垂体发育不良，畸形和中线影像学结合松散。
It is a heterogeneous condition defined loosely by any combination of optic nerve hypoplasia, pituitary hypoplasia, and midline neuroradiological malformations.
目的：检测无汗性外胚层发育不全患者的EDA基因的突变。
Objetive: to detect the gene mutation of a patient with anhidrotic ectodermal dysplasia.
目的：检测无汗性外胚层发育不全患者的EDA基因的突变。
Objetive: to detect the gene mutation of a patient with anhidrotic ectodermal dysplasia.
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