oligomelia diagnosis
寡端肢体诊断
oligomelia syndrome
寡端肢体综合征
suspect oligomelia
怀疑寡端肢体
oligomelia cases
寡端肢体病例
oligomelia presents
寡端肢体表现
oligomelia limb
寡端肢体肢体
severe oligomelia
严重的寡端肢体
oligomelia research
寡端肢体研究
oligomelia development
寡端肢体发育
oligomelia genetic
寡端肢体遗传
the infant was diagnosed with severe oligomelia in all four limbs.
婴儿被诊断出患有四肢严重的寡肢症。
oligomelia can be a sign of underlying genetic disorders.
寡肢症可能是潜在遗传性疾病的迹象。
prenatal ultrasound revealed the presence of oligomelia in the fetus.
产前超声检查显示胎儿患有寡肢症。
further investigation was needed to determine the cause of the oligomelia.
需要进一步调查以确定寡肢症的原因。
surgical intervention may be considered to improve function in cases of oligomelia.
在寡肢症病例中，可能需要考虑手术干预以改善功能。
the patient's medical history included a previous diagnosis of oligomelia.
患者的病史包括既往的寡肢症诊断。
oligomelia is a rare congenital condition characterized by shortened limbs.
寡肢症是一种罕见的先天性疾病，其特征是四肢缩短。
genetic testing was performed to rule out syndromes associated with oligomelia.
进行了基因检测以排除与寡肢症相关的综合征。
the severity of oligomelia varied significantly among the affected individuals.
受影响的个体中，寡肢症的严重程度差异很大。
physical therapy is often recommended for children with oligomelia.
物理治疗通常被推荐给患有寡肢症的儿童。
the radiographic findings confirmed the presence of oligomelia in the patient.
放射学检查结果证实了患者患有寡肢症。
oligomelia diagnosis
寡端肢体诊断
oligomelia syndrome
寡端肢体综合征
suspect oligomelia
怀疑寡端肢体
oligomelia cases
寡端肢体病例
oligomelia presents
寡端肢体表现
oligomelia limb
寡端肢体肢体
severe oligomelia
严重的寡端肢体
oligomelia research
寡端肢体研究
oligomelia development
寡端肢体发育
oligomelia genetic
寡端肢体遗传
the infant was diagnosed with severe oligomelia in all four limbs.
婴儿被诊断出患有四肢严重的寡肢症。
oligomelia can be a sign of underlying genetic disorders.
寡肢症可能是潜在遗传性疾病的迹象。
prenatal ultrasound revealed the presence of oligomelia in the fetus.
产前超声检查显示胎儿患有寡肢症。
further investigation was needed to determine the cause of the oligomelia.
需要进一步调查以确定寡肢症的原因。
surgical intervention may be considered to improve function in cases of oligomelia.
在寡肢症病例中，可能需要考虑手术干预以改善功能。
the patient's medical history included a previous diagnosis of oligomelia.
患者的病史包括既往的寡肢症诊断。
oligomelia is a rare congenital condition characterized by shortened limbs.
寡肢症是一种罕见的先天性疾病，其特征是四肢缩短。
genetic testing was performed to rule out syndromes associated with oligomelia.
进行了基因检测以排除与寡肢症相关的综合征。
the severity of oligomelia varied significantly among the affected individuals.
受影响的个体中，寡肢症的严重程度差异很大。
physical therapy is often recommended for children with oligomelia.
物理治疗通常被推荐给患有寡肢症的儿童。
the radiographic findings confirmed the presence of oligomelia in the patient.
放射学检查结果证实了患者患有寡肢症。
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