congenital acephaly
先天性無頭症
diagnosed with acephaly
診斷為無頭症
acephaly birth defect
無頭症先天缺陷
severe acephaly
嚴重無頭症
case of acephaly
無頭症病例
fetal acephaly
胎兒無頭症
signs of acephaly
無頭症症狀
occipital acephaly
枕部無頭症
partial acephaly
部分無頭症
infants with acephaly
患有無頭症的嬰兒
congenital acephaly is a rare developmental anomaly that results in the absence of a fully formed head.
先天性无头症是一種罕見的發育異常，導致頭部完全缺失。
the fetus was diagnosed with severe acephaly during the routine ultrasound examination.
胎兒在常規超聲波檢查中被診斷出患有嚴重的無頭症。
acephaly and other cephalic disorders are typically detected in the first trimester of pregnancy.
無頭症及其他頭部異常通常在懷孕的第一個 trimester 被發現。
researchers have studied acephaly in various animal models to understand developmental biology.
研究人員已在各種動物模型中研究無頭症，以了解發育生物學。
lethal acephaly prevents survival beyond the embryonic or neonatal period in most cases.
致命性無頭症在大多數情況下會阻止胚胎或新生兒期後的生存。
the medical literature documents several instances of acephaly occurring in mammalian species.
醫學文獻記載了多個哺乳動物物種中發生無頭症的案例。
acephaly is often associated with other severe congenital malformations affecting the central nervous system.
無頭症通常與影響中樞神經系統的其他嚴重先天性畸形有關。
genetic mutations have been linked to some cases of acephaly in experimental studies.
實驗研究已將基因突變與某些無頭症病例聯繫起來。
parents receive genetic counseling when acephaly is identified through prenatal diagnostic testing.
當通過產前診斷測試確認無頭症時，父母會接受遺傳諮詢。
veterinary pathologists occasionally encounter acephaly in domestic animal populations.
獸醫病理學家偶爾會在家畜群體中遇到無頭症。
the embryonic development of acephaly begins during the early stages of neurulation.
無頭症的胚胎發育是在神經管形成的早期階段開始的。
complete acephaly is incompatible with extrauterine life in vertebrates.
完全無頭症在脊椎動物中與體外生命不相容。
ultrasonographic detection of acephaly allows families to make informed decisions about pregnancy management.
無頭症的超聲波檢測使家庭能夠做出有關懷孕管理的知情決定。
scientists continue to investigate the molecular mechanisms underlying acephaly and related conditions.
科學家們繼續研究導致無頭症及其相關疾病的分子機制。
congenital acephaly
先天性無頭症
diagnosed with acephaly
診斷為無頭症
acephaly birth defect
無頭症先天缺陷
severe acephaly
嚴重無頭症
case of acephaly
無頭症病例
fetal acephaly
胎兒無頭症
signs of acephaly
無頭症症狀
occipital acephaly
枕部無頭症
partial acephaly
部分無頭症
infants with acephaly
患有無頭症的嬰兒
congenital acephaly is a rare developmental anomaly that results in the absence of a fully formed head.
先天性无头症是一種罕見的發育異常，導致頭部完全缺失。
the fetus was diagnosed with severe acephaly during the routine ultrasound examination.
胎兒在常規超聲波檢查中被診斷出患有嚴重的無頭症。
acephaly and other cephalic disorders are typically detected in the first trimester of pregnancy.
無頭症及其他頭部異常通常在懷孕的第一個 trimester 被發現。
researchers have studied acephaly in various animal models to understand developmental biology.
研究人員已在各種動物模型中研究無頭症，以了解發育生物學。
lethal acephaly prevents survival beyond the embryonic or neonatal period in most cases.
致命性無頭症在大多數情況下會阻止胚胎或新生兒期後的生存。
the medical literature documents several instances of acephaly occurring in mammalian species.
醫學文獻記載了多個哺乳動物物種中發生無頭症的案例。
acephaly is often associated with other severe congenital malformations affecting the central nervous system.
無頭症通常與影響中樞神經系統的其他嚴重先天性畸形有關。
genetic mutations have been linked to some cases of acephaly in experimental studies.
實驗研究已將基因突變與某些無頭症病例聯繫起來。
parents receive genetic counseling when acephaly is identified through prenatal diagnostic testing.
當通過產前診斷測試確認無頭症時，父母會接受遺傳諮詢。
veterinary pathologists occasionally encounter acephaly in domestic animal populations.
獸醫病理學家偶爾會在家畜群體中遇到無頭症。
the embryonic development of acephaly begins during the early stages of neurulation.
無頭症的胚胎發育是在神經管形成的早期階段開始的。
complete acephaly is incompatible with extrauterine life in vertebrates.
完全無頭症在脊椎動物中與體外生命不相容。
ultrasonographic detection of acephaly allows families to make informed decisions about pregnancy management.
無頭症的超聲波檢測使家庭能夠做出有關懷孕管理的知情決定。
scientists continue to investigate the molecular mechanisms underlying acephaly and related conditions.
科學家們繼續研究導致無頭症及其相關疾病的分子機制。
探索常見搜尋詞彙