His children were dwarfed by insufficient food.

他的儿女因营养良而发。

So this fetus presented seeral signs of trisomy 21, including the hypoplasia of the nasal bone, hypodontia, micrognathia, and hypospadias.

这样，本例胎儿显示21三体的若干征象：包括鼻骨发、牙发、小颌和尿道下裂。

19 cases had dilated seminal vesicles,19 seminal vesicle agenesis,9 seminal vesiculitis and 5 dilation of the ejaculatory duct.

伴有精囊腺扩张者19例,精囊缺如或发者19例,精囊炎9例,射精管扩张5例。

It is suggested that lumbosacral agenesis, a severe congenital defect, might be one of the anomalies of diabetic embryopathy.

病例显示腰荐椎发可能是母亲糖尿病所导致胚胎病变的一种，且无论有无接受胰岛素治疗，形仍可能形成。

At 30 weeks an MRI was done. The two lungs were present. A right pulmonary agenesia was eliminated. A diastematomyelia was eliminated either.

孕30周行MRI检查发现两侧肺脏，排除右肺发和脊髓纵裂。

Four patients with blind end of vas and vessels proximal to the internal inquinal ring were planned for orchiectomy or simple or staged orchidopexy depending on clinical situations.

六位病人可见正常之输精管及精索血管进入内复股沟环，仍接受复股沟探查手术，其中四位病人位于患侧仍未发现睪丸，另两位病人则发现发之睪丸。

His children were dwarfed by insufficient food.

他的儿女因营养不良而发育不全。

So this fetus presented seeral signs of trisomy 21, including the hypoplasia of the nasal bone, hypodontia, micrognathia, and hypospadias.

这样，本例胎儿显示21三体的若干征象：包括鼻骨发育不全、牙发育不全、小颌和尿道下裂。

19 cases had dilated seminal vesicles,19 seminal vesicle agenesis,9 seminal vesiculitis and 5 dilation of the ejaculatory duct.

伴有囊腺扩张者19例,囊缺如或发育不全者19例,囊炎9例,射管扩张5例。

It is suggested that lumbosacral agenesis, a severe congenital defect, might be one of the anomalies of diabetic embryopathy.

病例显示腰荐椎发育不全可能是母亲糖尿病所导致胚胎病变的一种，且无论有无接受胰岛素治疗，先天畸形仍可能形成。

At 30 weeks an MRI was done. The two lungs were present. A right pulmonary agenesia was eliminated. A diastematomyelia was eliminated either.

孕30周行MRI检查发现两侧肺脏，排除右肺发育不全和脊髓纵裂。

Four patients with blind end of vas and vessels proximal to the internal inquinal ring were planned for orchiectomy or simple or staged orchidopexy depending on clinical situations.

六位病人可见正常之输管血管进入内复股沟环，仍接受复股沟探查手术，其中四位病人位于患侧仍未发现睪丸，另两位病人则发现发育不全之睪丸。

His children were dwarfed by insufficient food.

他的儿女因营养良而全。

So this fetus presented seeral signs of trisomy 21, including the hypoplasia of the nasal bone, hypodontia, micrognathia, and hypospadias.

这样，本例胎儿显示21三体的若干征象：包括鼻骨全、牙全、小颌和尿道下裂。

19 cases had dilated seminal vesicles,19 seminal vesicle agenesis,9 seminal vesiculitis and 5 dilation of the ejaculatory duct.

伴有精囊腺扩张者19例,精囊缺如或全者19例,精囊炎9例,射精管扩张5例。

It is suggested that lumbosacral agenesis, a severe congenital defect, might be one of the anomalies of diabetic embryopathy.

病例显示腰荐椎全可能是母亲糖尿病所导致胚胎病变的一种，且无论有无接受胰岛素治疗，先仍可能成。

At 30 weeks an MRI was done. The two lungs were present. A right pulmonary agenesia was eliminated. A diastematomyelia was eliminated either.

孕30周行MRI检查现两侧肺脏，排除右肺全和脊髓纵裂。

Four patients with blind end of vas and vessels proximal to the internal inquinal ring were planned for orchiectomy or simple or staged orchidopexy depending on clinical situations.

六位病人可见正常之输精管及精索血管进入内复股沟环，仍接受复股沟探查手术，其中四位病人位于患侧仍未现睪丸，另两位病人则现全之睪丸。

His children were dwarfed by insufficient food.

他的儿女因营养不良而不全。

So this fetus presented seeral signs of trisomy 21, including the hypoplasia of the nasal bone, hypodontia, micrognathia, and hypospadias.

这样，本例胎儿显示21三体的若干征象：包括鼻不全、牙不全、小颌和尿道下裂。

19 cases had dilated seminal vesicles,19 seminal vesicle agenesis,9 seminal vesiculitis and 5 dilation of the ejaculatory duct.

伴有精囊腺扩张者19例,精囊缺如或不全者19例,精囊炎9例,射精管扩张5例。

It is suggested that lumbosacral agenesis, a severe congenital defect, might be one of the anomalies of diabetic embryopathy.

病例显示腰荐椎不全可能是母亲糖尿病所导致胚胎病变的一种，且无论有无接受胰岛素治疗，先天可能成。

At 30 weeks an MRI was done. The two lungs were present. A right pulmonary agenesia was eliminated. A diastematomyelia was eliminated either.

孕30周行MRI检查现两侧肺脏，排除右肺不全和脊髓纵裂。

Four patients with blind end of vas and vessels proximal to the internal inquinal ring were planned for orchiectomy or simple or staged orchidopexy depending on clinical situations.

六位病人可见正常之输精管及精索血管进入内复股沟环，接受复股沟探查手术，其中四位病人位于患侧未现睪丸，另两位病人则现不全之睪丸。

His children were dwarfed by insufficient food.

他的儿女因营养良而发。

So this fetus presented seeral signs of trisomy 21, including the hypoplasia of the nasal bone, hypodontia, micrognathia, and hypospadias.

这样，本例胎儿显示21三体的若干征象：包括鼻骨发、牙发、小颌和尿道下裂。

19 cases had dilated seminal vesicles,19 seminal vesicle agenesis,9 seminal vesiculitis and 5 dilation of the ejaculatory duct.

伴有精囊腺扩张者19例,精囊缺如或发者19例,精囊炎9例,射精管扩张5例。

It is suggested that lumbosacral agenesis, a severe congenital defect, might be one of the anomalies of diabetic embryopathy.

病例显示腰荐椎发可能是母亲糖尿病所导致胚胎病变的一种，且无论有无接受胰岛素治疗，形仍可能形成。

At 30 weeks an MRI was done. The two lungs were present. A right pulmonary agenesia was eliminated. A diastematomyelia was eliminated either.

孕30周行MRI检查发现两侧肺脏，排除右肺发和脊髓纵裂。

Four patients with blind end of vas and vessels proximal to the internal inquinal ring were planned for orchiectomy or simple or staged orchidopexy depending on clinical situations.

六位病人可见正常之输精管及精索血管进入内复股沟环，仍接受复股沟探查手术，其中四位病人位于患侧仍未发现睪丸，另两位病人则发现发之睪丸。

His children were dwarfed by insufficient food.

他的儿女因营养不良而育不全。

So this fetus presented seeral signs of trisomy 21, including the hypoplasia of the nasal bone, hypodontia, micrognathia, and hypospadias.

这样，本例胎儿显21的若干征象：包括鼻骨育不全、牙育不全、小颌和尿道下裂。

19 cases had dilated seminal vesicles,19 seminal vesicle agenesis,9 seminal vesiculitis and 5 dilation of the ejaculatory duct.

伴有精囊腺扩张者19例,精囊缺如或育不全者19例,精囊炎9例,射精管扩张5例。

It is suggested that lumbosacral agenesis, a severe congenital defect, might be one of the anomalies of diabetic embryopathy.

病例显腰荐椎育不全可能是母亲糖尿病所导致胚胎病变的一种，且无论有无接受胰岛素治疗，先天畸形仍可能形成。

At 30 weeks an MRI was done. The two lungs were present. A right pulmonary agenesia was eliminated. A diastematomyelia was eliminated either.

孕30周行MRI检两侧肺脏，排除右肺育不全和脊髓纵裂。

Four patients with blind end of vas and vessels proximal to the internal inquinal ring were planned for orchiectomy or simple or staged orchidopexy depending on clinical situations.

六位病人可见正常之输精管及精索血管进入内复股沟环，仍接受复股沟探手术，其中四位病人位于患侧仍未睪丸，另两位病人则育不全之睪丸。

His children were dwarfed by insufficient food.

儿女因营养不良而发育不全。

So this fetus presented seeral signs of trisomy 21, including the hypoplasia of the nasal bone, hypodontia, micrognathia, and hypospadias.

这样，本例胎儿显示21三体若干征象：包括鼻骨发育不全、牙发育不全、小颌和尿道下裂。

19 cases had dilated seminal vesicles,19 seminal vesicle agenesis,9 seminal vesiculitis and 5 dilation of the ejaculatory duct.

伴有精囊腺扩张者19例,精囊缺如或发育不全者19例,精囊炎9例,射精管扩张5例。

It is suggested that lumbosacral agenesis, a severe congenital defect, might be one of the anomalies of diabetic embryopathy.

例显示腰荐椎发育不全能是母亲糖尿所导致胚胎变一种，且无论有无接受胰岛素治疗，先天畸形仍能形成。

At 30 weeks an MRI was done. The two lungs were present. A right pulmonary agenesia was eliminated. A diastematomyelia was eliminated either.

孕30周行MRI检查发现两侧肺脏，排除右肺发育不全和脊髓纵裂。

Four patients with blind end of vas and vessels proximal to the internal inquinal ring were planned for orchiectomy or simple or staged orchidopexy depending on clinical situations.

六位见正常之输精管及精索血管进入内复股沟环，仍接受复股沟探查手术，其中四位位于患侧仍未发现睪丸，另两位则发现发育不全之睪丸。

His children were dwarfed by insufficient food.

他的儿女因营养不良而发育不全。

So this fetus presented seeral signs of trisomy 21, including the hypoplasia of the nasal bone, hypodontia, micrognathia, and hypospadias.

这样，本胎儿显示21三体的若干征象：包括鼻骨发育不全、牙发育不全、小颌和尿道下裂。

19 cases had dilated seminal vesicles,19 seminal vesicle agenesis,9 seminal vesiculitis and 5 dilation of the ejaculatory duct.

伴有腺扩张者19,缺如或发育不全者19,炎9,射管扩张5。

It is suggested that lumbosacral agenesis, a severe congenital defect, might be one of the anomalies of diabetic embryopathy.

病显示腰荐椎发育不全可能是母亲糖尿病所胚胎病变的一种，且无论有无接受胰岛素治疗，先天畸形仍可能形成。

At 30 weeks an MRI was done. The two lungs were present. A right pulmonary agenesia was eliminated. A diastematomyelia was eliminated either.

孕30周行MRI检查发现两侧肺脏，排除右肺发育不全和脊髓纵裂。

Four patients with blind end of vas and vessels proximal to the internal inquinal ring were planned for orchiectomy or simple or staged orchidopexy depending on clinical situations.

六位病人可见正常之输管及索血管进入内复股沟环，仍接受复股沟探查手术，其中四位病人位于患侧仍未发现睪丸，另两位病人则发现发育不全之睪丸。

His children were dwarfed by insufficient food.

他的儿女因营而发育全。

So this fetus presented seeral signs of trisomy 21, including the hypoplasia of the nasal bone, hypodontia, micrognathia, and hypospadias.

这样，本例胎儿显示21三体的若干征象：包括鼻骨发育全、牙发育全、小颌尿道下裂。

19 cases had dilated seminal vesicles,19 seminal vesicle agenesis,9 seminal vesiculitis and 5 dilation of the ejaculatory duct.

伴有精囊腺扩张者19例,精囊缺如或发育全者19例,精囊炎9例,射精管扩张5例。

It is suggested that lumbosacral agenesis, a severe congenital defect, might be one of the anomalies of diabetic embryopathy.

病例显示腰荐椎发育全可能是母亲糖尿病所导致胚胎病变的一种，且无论有无接受胰岛素治疗，先天畸形仍可能形成。

At 30 weeks an MRI was done. The two lungs were present. A right pulmonary agenesia was eliminated. A diastematomyelia was eliminated either.

孕30周行MRI检查发现两侧肺脏，排除右肺发育全纵裂。

Four patients with blind end of vas and vessels proximal to the internal inquinal ring were planned for orchiectomy or simple or staged orchidopexy depending on clinical situations.

六位病人可见正常之输精管及精索血管进入内复股沟环，仍接受复股沟探查手术，其中四位病人位于患侧仍未发现睪丸，另两位病人则发现发育全之睪丸。

His children were dwarfed by insufficient food.

他的儿女因营养良。

So this fetus presented seeral signs of trisomy 21, including the hypoplasia of the nasal bone, hypodontia, micrognathia, and hypospadias.

这样，本例胎儿显示21三体的若干征象：包括鼻骨、牙、小颌和尿道下裂。

19 cases had dilated seminal vesicles,19 seminal vesicle agenesis,9 seminal vesiculitis and 5 dilation of the ejaculatory duct.

伴有精囊腺扩张者19例,精囊缺如或者19例,精囊炎9例,射精管扩张5例。

It is suggested that lumbosacral agenesis, a severe congenital defect, might be one of the anomalies of diabetic embryopathy.

病例显示腰荐椎可能是母亲糖尿病所导致胚胎病变的一种，且无论有无接受胰岛素治疗，先天畸形仍可能形成。

At 30 weeks an MRI was done. The two lungs were present. A right pulmonary agenesia was eliminated. A diastematomyelia was eliminated either.

孕30周行MRI检查现两侧肺脏，排除右肺和脊髓纵裂。

Four patients with blind end of vas and vessels proximal to the internal inquinal ring were planned for orchiectomy or simple or staged orchidopexy depending on clinical situations.

六位病人可见正常之输精管及精索血管进入内复股沟环，仍接受复股沟探查手术，其中四位病人位于患侧仍未现睪丸，另两位病人则现之睪丸。