oligomelia diagnosis
少肢症診斷
oligomelia syndrome
少肢症候群
suspect oligomelia
懷疑少肢症
oligomelia cases
少肢症病例
oligomelia presents
少肢症表現
oligomelia limb
少肢症肢體
severe oligomelia
嚴重少肢症
oligomelia research
少肢症研究
oligomelia development
少肢症發展
oligomelia genetic
少肢症遺傳
the infant was diagnosed with severe oligomelia in all four limbs.
嬰兒被診斷為四肢嚴重肢體發育不全。
oligomelia can be a sign of underlying genetic disorders.
肢體發育不全可能是潛在遺傳疾病的一個徵兆。
prenatal ultrasound revealed the presence of oligomelia in the fetus.
產前超聲波檢查顯示胎兒有肢體發育不全的情況。
further investigation was needed to determine the cause of the oligomelia.
需要進一步檢查以確定肢體發育不全的原因。
surgical intervention may be considered to improve function in cases of oligomelia.
在肢體發育不全的情況下，可能需要考慮手術干預以改善功能。
the patient's medical history included a previous diagnosis of oligomelia.
患者的病史中包括先前診斷為肢體發育不全。
oligomelia is a rare congenital condition characterized by shortened limbs.
肢體發育不全是罕見的先天性疾病，特徵是四肢短縮。
genetic testing was performed to rule out syndromes associated with oligomelia.
進行遺傳測試以排除與肢體發育不全相關的綜合徵。
the severity of oligomelia varied significantly among the affected individuals.
受影響個體的肢體發育不全嚴重程度差異很大。
physical therapy is often recommended for children with oligomelia.
對於有肢體發育不全的兒童，通常會建議進行物理治療。
the radiographic findings confirmed the presence of oligomelia in the patient.
放射檢查結果確認患者存在肢體發育不全。
oligomelia diagnosis
少肢症診斷
oligomelia syndrome
少肢症候群
suspect oligomelia
懷疑少肢症
oligomelia cases
少肢症病例
oligomelia presents
少肢症表現
oligomelia limb
少肢症肢體
severe oligomelia
嚴重少肢症
oligomelia research
少肢症研究
oligomelia development
少肢症發展
oligomelia genetic
少肢症遺傳
the infant was diagnosed with severe oligomelia in all four limbs.
嬰兒被診斷為四肢嚴重肢體發育不全。
oligomelia can be a sign of underlying genetic disorders.
肢體發育不全可能是潛在遺傳疾病的一個徵兆。
prenatal ultrasound revealed the presence of oligomelia in the fetus.
產前超聲波檢查顯示胎兒有肢體發育不全的情況。
further investigation was needed to determine the cause of the oligomelia.
需要進一步檢查以確定肢體發育不全的原因。
surgical intervention may be considered to improve function in cases of oligomelia.
在肢體發育不全的情況下，可能需要考慮手術干預以改善功能。
the patient's medical history included a previous diagnosis of oligomelia.
患者的病史中包括先前診斷為肢體發育不全。
oligomelia is a rare congenital condition characterized by shortened limbs.
肢體發育不全是罕見的先天性疾病，特徵是四肢短縮。
genetic testing was performed to rule out syndromes associated with oligomelia.
進行遺傳測試以排除與肢體發育不全相關的綜合徵。
the severity of oligomelia varied significantly among the affected individuals.
受影響個體的肢體發育不全嚴重程度差異很大。
physical therapy is often recommended for children with oligomelia.
對於有肢體發育不全的兒童，通常會建議進行物理治療。
the radiographic findings confirmed the presence of oligomelia in the patient.
放射檢查結果確認患者存在肢體發育不全。
探索常見搜尋詞彙