acromyotonia diagnosis
肢带肌张力障碍诊断
acromyotonias presented
inherited acromyotonia
遗传性肢带肌张力障碍
acromyotonia treatment
肢带肌张力障碍治疗
acromyotonias include
rare acromyotonia
罕见肢带肌张力障碍
acromyotonia with
伴有肢带肌张力障碍
acromyotonias are
congenital acromyotonia
先天性肢带肌张力障碍
acromyotonias often
the patient was diagnosed with congenital acromyotonias affecting both hands and feet.
患者被诊断为先天性肢端肥大症，影响双手和双脚。
hereditary acromyotonias often manifest in early childhood with muscle stiffness.
遗传性肢端肥大症通常在儿童早期表现为肌肉僵硬。
chronic acromyotonias requires long-term management and physical therapy.
慢性肢端肥大症需要长期管理和物理治疗。
the medical team studied several cases of severe acromyotonias in the clinical trial.
医疗团队在临床试验中研究了多例严重的肢端肥大症病例。
symptoms of acromyotonias include persistent muscle contractions in the extremities.
肢端肥大症的症状包括四肢的持续肌肉收缩。
treatment options for acromyotonias have improved significantly over the past decade.
在过去十年中，肢端肥大症的治疗方案有了显著改善。
patients with acromyotonias often experience difficulty with fine motor skills.
肢端肥大症患者通常在精细动作技能上存在困难。
the neurologist specialized in diagnosing rare neuromuscular disorders including acromyotonias.
这位神经科医生专长于诊断包括肢端肥大症在内的罕见神经肌肉疾病。
early intervention can help manage the progression of acromyotonias effectively.
早期干预有助于有效管理肢端肥大症的进展。
acromyotonias may be associated with underlying genetic mutations in some cases.
在某些情况下，肢端肥大症可能与潜在的基因突变有关。
genetic testing can confirm suspected cases of hereditary acromyotonias.
基因检测可以确认遗传性肢端肥大症的疑似病例。
physical therapy exercises are essential for patients suffering from acromyotonias.
对于患有肢端肥大症的患者来说，物理治疗运动是必不可少的。
acromyotonia diagnosis
肢带肌张力障碍诊断
acromyotonias presented
inherited acromyotonia
遗传性肢带肌张力障碍
acromyotonia treatment
肢带肌张力障碍治疗
acromyotonias include
rare acromyotonia
罕见肢带肌张力障碍
acromyotonia with
伴有肢带肌张力障碍
acromyotonias are
congenital acromyotonia
先天性肢带肌张力障碍
acromyotonias often
the patient was diagnosed with congenital acromyotonias affecting both hands and feet.
患者被诊断为先天性肢端肥大症，影响双手和双脚。
hereditary acromyotonias often manifest in early childhood with muscle stiffness.
遗传性肢端肥大症通常在儿童早期表现为肌肉僵硬。
chronic acromyotonias requires long-term management and physical therapy.
慢性肢端肥大症需要长期管理和物理治疗。
the medical team studied several cases of severe acromyotonias in the clinical trial.
医疗团队在临床试验中研究了多例严重的肢端肥大症病例。
symptoms of acromyotonias include persistent muscle contractions in the extremities.
肢端肥大症的症状包括四肢的持续肌肉收缩。
treatment options for acromyotonias have improved significantly over the past decade.
在过去十年中，肢端肥大症的治疗方案有了显著改善。
patients with acromyotonias often experience difficulty with fine motor skills.
肢端肥大症患者通常在精细动作技能上存在困难。
the neurologist specialized in diagnosing rare neuromuscular disorders including acromyotonias.
这位神经科医生专长于诊断包括肢端肥大症在内的罕见神经肌肉疾病。
early intervention can help manage the progression of acromyotonias effectively.
早期干预有助于有效管理肢端肥大症的进展。
acromyotonias may be associated with underlying genetic mutations in some cases.
在某些情况下，肢端肥大症可能与潜在的基因突变有关。
genetic testing can confirm suspected cases of hereditary acromyotonias.
基因检测可以确认遗传性肢端肥大症的疑似病例。
physical therapy exercises are essential for patients suffering from acromyotonias.
对于患有肢端肥大症的患者来说，物理治疗运动是必不可少的。
探索常用高频词汇