encephaloceles present
脑脑膨出
diagnosing encephaloceles
诊断脑膨出
encephaloceles risk
脑膨出风险
severe encephaloceles
严重的脑膨出
encephaloceles screening
脑膨出筛查
encephaloceles cases
脑膨出病例
detecting encephaloceles
检测脑膨出
encephaloceles surgery
脑膨出手术
encephaloceles development
脑膨出发展
encephaloceles research
脑膨出研究
prenatal ultrasound screenings often detect the presence of encephaloceles.
产前超声筛查通常会检测到脑膨出症的存在。
surgical intervention is frequently necessary to repair encephaloceles and improve neurological function.
手术干预经常有必要以修复脑膨出症并改善神经功能。
encephaloceles can be associated with other birth defects, such as spina bifida.
脑膨出症可能与其他先天缺陷有关，例如脊柱裂。
the severity of encephaloceles varies widely, ranging from mild to severe.
脑膨出症的严重程度差异很大，从轻微到严重不等。
genetic mutations are sometimes implicated in the development of encephaloceles.
遗传突变有时与脑膨出症的发育有关。
early diagnosis of encephaloceles is crucial for optimal management and care.
脑膨出症的早期诊断对于最佳管理和护理至关重要。
families affected by encephaloceles often require genetic counseling.
受脑膨出症影响的家庭通常需要遗传咨询。
the incidence of encephaloceles is estimated to be around 1 in 2,500 births.
据估计，脑膨出症的发病率约为每2500个新生儿发生一次。
neuroimaging studies, like mri, are essential for evaluating the extent of encephaloceles.
神经影像学研究，如mri，对于评估脑膨出症的程度至关重要。
encephaloceles can lead to significant developmental delays and disabilities.
脑膨出症会导致重大的发育迟缓和残疾。
postnatal care for infants with encephaloceles focuses on maximizing their potential.
患有脑膨出症的婴儿的产后护理侧重于最大限度地发挥他们的潜力。
encephaloceles present
脑脑膨出
diagnosing encephaloceles
诊断脑膨出
encephaloceles risk
脑膨出风险
severe encephaloceles
严重的脑膨出
encephaloceles screening
脑膨出筛查
encephaloceles cases
脑膨出病例
detecting encephaloceles
检测脑膨出
encephaloceles surgery
脑膨出手术
encephaloceles development
脑膨出发展
encephaloceles research
脑膨出研究
prenatal ultrasound screenings often detect the presence of encephaloceles.
产前超声筛查通常会检测到脑膨出症的存在。
surgical intervention is frequently necessary to repair encephaloceles and improve neurological function.
手术干预经常有必要以修复脑膨出症并改善神经功能。
encephaloceles can be associated with other birth defects, such as spina bifida.
脑膨出症可能与其他先天缺陷有关，例如脊柱裂。
the severity of encephaloceles varies widely, ranging from mild to severe.
脑膨出症的严重程度差异很大，从轻微到严重不等。
genetic mutations are sometimes implicated in the development of encephaloceles.
遗传突变有时与脑膨出症的发育有关。
early diagnosis of encephaloceles is crucial for optimal management and care.
脑膨出症的早期诊断对于最佳管理和护理至关重要。
families affected by encephaloceles often require genetic counseling.
受脑膨出症影响的家庭通常需要遗传咨询。
the incidence of encephaloceles is estimated to be around 1 in 2,500 births.
据估计，脑膨出症的发病率约为每2500个新生儿发生一次。
neuroimaging studies, like mri, are essential for evaluating the extent of encephaloceles.
神经影像学研究，如mri，对于评估脑膨出症的程度至关重要。
encephaloceles can lead to significant developmental delays and disabilities.
脑膨出症会导致重大的发育迟缓和残疾。
postnatal care for infants with encephaloceles focuses on maximizing their potential.
患有脑膨出症的婴儿的产后护理侧重于最大限度地发挥他们的潜力。
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