发育异常

The results showed that there were immature cells (2%-10%) and erythroblast, and puncture of bone marrow revealed myelodysplastic features involving multiple hemopoietic lineages in bone marrow of 19 patients.

结果表明： M6患者的外周血中均可见幼稚细胞（2％-10％）及有核红细胞，骨髓穿刺细胞学检查显示19例伴有多系细胞发育异常，累及二系细胞或三系细胞。

Assignment of SRY as the testis-determining factor in eutherian mammals is supported by molecular analysis of cytogenetic sex reversal (i.e., XX males and XY females) and by complementary studies of transgenic murine models.

Sry转基因小鼠的产生和对包括XX男性及XY女性等多种性分化及发育异常患者的研究，都支持SRY基因是TDF基因及其在性别决定中的开关控制作用。

There was no evidenceof dysplasia within the fascicle of any nerve.

没有证据表明在任何神经束存在发育异常。

Cerebral CT scan has significant diagnostic value in cerebral palsy children.Abnormal fetation perhaps is the main cause.

脑瘫的CT检查有极高的价值；胚胎期发育异常可能是脑瘫的主要病因。

Holoprosencephaly is the most common abnormality of the deelopment of the forebrain in humans.

前脑无裂畸形是人类前脑发育异常中最常见的类型。

One patient had transient insufficient blood supply of the glans and recovered gradually by symptomatic treatment.

结果：26例患者都有不同程度的阴茎浅筋膜发育异常，22例患者行阴茎海绵体松解牵拉术，10例行maizels术。

Results All the patients of this group had characteristics of ineffective hematopoiesis.

结果：所有患者均存在不同程度的血细胞发育异常的形态学表现。

Intracal malacoma 32 cases,cyst of pellucid septal cave 19 cases ,alba dysplasia 16 cases,grey matter heterotopia 7cases,porencephaly...

脑瘫的CT检查有极高的价值：胚胎期发育异常和新生儿窒息可能是该地区小儿脑瘫的主要病因。

Neurodevelopmental disability is proportionate to the thickness of the heterotopic "band." The manifestations of this x-linked disease are more drastic than SEH; males suffer from lissencephaly, while females suffer from band heterotopia.

神经发育异常的严重程度取决于灰质带的厚度。。X-连锁性病变的现象比SEH更明显，男性表现为无脑回，女性表现为带状异位。

Results CTVE could clearly demonstrate the shape,size,and relation of the normal auditory ossicular chain.A visualization rate of malleus,incus,and incudomalleal articulation was 100%,and was 32% for the stapedial footplate.However,in only 21% could the anterior and posterior crura of stapes be distinguished.Cholesteatoma was found in 12 cases with chronic otitis media,in which CTVE demonstrated varying degrees of destruction of the auditory ossicle.In 1 case with congenital anomaly,ossicle dysplasia was seen.

结果 CTVE能清楚显示正常听骨链的形态、大小及相互关系，锤骨、砧骨及锤砧关节的显示率为100%(38/38)，镫骨底板的显示率为32%(12/38)，只有21%(8/38)可以分辨镫骨的前、后脚；18例中耳炎患者中12例胆脂瘤形成，CTVE上有不同程度的听小骨破坏。1例中耳畸形显示听骨链发育异常。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。