acromicry condition
肢端肥大症病情
suffering from acromicry
患有肢端肥大症
acromicry symptoms
肢端肥大症症状
treating acromicry
治疗肢端肥大症
acromicry diagnosis
肢端肥大症诊断
acromicry patient
肢端肥大症患者
acromicry treatment
肢端肥大症治疗
acromicry research
肢端肥大症研究
acromicry effects
肢端肥大症影响
acromicry cause
肢端肥大症病因
the doctor noted the patient's distinct facial acromicry during the physical examination.
医生在体格检查中注意到了患者明显的面部肢端过小症。
acromicry is often identified by abnormally small hands and feet in affected individuals.
肢端过小症通常通过受影响个体的手和脚异常小来识别。
genetic testing helps determine if the observed acromicry is linked to a specific syndrome.
基因检测有助于观察到的肢端过小症是否与特定综合征有关。
researchers compared the clinical data to better understand the causes of acromicry.
研究人员比较了临床数据以更好地了解肢端过小症的病因。
unlike acromegaly, acromicry involves a reduction in the size of the extremities.
与肢端肥大症不同，肢端过小症涉及四肢尺寸的缩小。
the medical student wrote a thesis on the rare symptoms associated with acromicry.
这名医学生写了一篇关于与肢端过小症相关的罕见症状的论文。
endocrinologists look for hormonal imbalances that might contribute to the development of acromicry.
内分泌学家寻找可能导致肢端过小症发展的激素失衡。
severe cases of acromicry can affect fine motor skills and dexterity.
严重的肢端过小症会影响精细运动技能和灵巧度。
the textbook illustrates the skeletal differences caused by congenital acromicry.
教科书展示了先天性肢端过小症引起的骨骼差异。
pediatricians monitor growth patterns to detect early signs of acromicry in children.
儿科医生监测生长模式以检测儿童肢端过小症的早期迹象。
the diagnosis of acromicry requires a careful analysis of skeletal development.
肢端过小症的诊断需要仔细分析骨骼发育情况。
pathologists studied the tissue samples to find the biological markers of acromicry.
病理学家研究组织样本以寻找肢端过小症的生物标志物。
acromicry condition
肢端肥大症病情
suffering from acromicry
患有肢端肥大症
acromicry symptoms
肢端肥大症症状
treating acromicry
治疗肢端肥大症
acromicry diagnosis
肢端肥大症诊断
acromicry patient
肢端肥大症患者
acromicry treatment
肢端肥大症治疗
acromicry research
肢端肥大症研究
acromicry effects
肢端肥大症影响
acromicry cause
肢端肥大症病因
the doctor noted the patient's distinct facial acromicry during the physical examination.
医生在体格检查中注意到了患者明显的面部肢端过小症。
acromicry is often identified by abnormally small hands and feet in affected individuals.
肢端过小症通常通过受影响个体的手和脚异常小来识别。
genetic testing helps determine if the observed acromicry is linked to a specific syndrome.
基因检测有助于观察到的肢端过小症是否与特定综合征有关。
researchers compared the clinical data to better understand the causes of acromicry.
研究人员比较了临床数据以更好地了解肢端过小症的病因。
unlike acromegaly, acromicry involves a reduction in the size of the extremities.
与肢端肥大症不同，肢端过小症涉及四肢尺寸的缩小。
the medical student wrote a thesis on the rare symptoms associated with acromicry.
这名医学生写了一篇关于与肢端过小症相关的罕见症状的论文。
endocrinologists look for hormonal imbalances that might contribute to the development of acromicry.
内分泌学家寻找可能导致肢端过小症发展的激素失衡。
severe cases of acromicry can affect fine motor skills and dexterity.
严重的肢端过小症会影响精细运动技能和灵巧度。
the textbook illustrates the skeletal differences caused by congenital acromicry.
教科书展示了先天性肢端过小症引起的骨骼差异。
pediatricians monitor growth patterns to detect early signs of acromicry in children.
儿科医生监测生长模式以检测儿童肢端过小症的早期迹象。
the diagnosis of acromicry requires a careful analysis of skeletal development.
肢端过小症的诊断需要仔细分析骨骼发育情况。
pathologists studied the tissue samples to find the biological markers of acromicry.
病理学家研究组织样本以寻找肢端过小症的生物标志物。
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