n.软骨营养障碍

Chondrodysplasia is a genetic disorder that affects the development of bones, particularly in the joints.
骨软骨发育不良是一种影响骨骼，特别是关节发育的遗传性疾病。
The child was diagnosed with chondrodysplasia at birth due to its short stature and bowed legs.
这个孩子出生时被诊断为患有骨软骨发育不良，因为他的身高矮小和腿型弯曲。
Hereditary chondrodysplasia is inherited through an autosomal dominant pattern, meaning one affected parent can pass it on to their offspring.
遗传性骨软骨发育不良是通过常染色体显性遗传的，意味着受影响的父母会将其传递给他们的后代。
Radiographs showed characteristic features of chondrodysplasia, such as short limbs and thickened cartilage.
X光显示了骨软骨发育不良的典型特征，如短肢和增厚的软骨。
Early intervention for chondrodysplasia is crucial to prevent complications like arthritis and skeletal deformities.
对于骨软骨发育不良的早期干预对于防止关节炎和骨骼畸形至关重要。
Treatment for chondrodysplasia often involves physical therapy, pain management, and in severe cases, surgical interventions.
骨软骨发育不良的治疗通常包括物理疗法、疼痛管理，以及在严重情况下进行手术干预。
The genetic counselor provided education on the risks and management options for chondrodysplasia in their family.
遗传咨询师为他们家庭提供了关于骨软骨发育不良的风险和管理选择的教育。
Scientists are researching new therapies for chondrodysplasia, hoping to find a cure or at least improve quality of life for those affected.
科学家正在研究针对骨软骨发育不良的新疗法，希望能找到治愈或至少提高患者生活质量的方法。
In rare cases, chondrodysplasia can lead to respiratory issues due to abnormalities in the ribcage structure.
在极少数情况下，骨软骨发育不良可能导致呼吸道问题，因为胸腔结构异常。
A support group for individuals with chondrodysplasia helps them cope with the challenges and share experiences related to the condition.
针对骨软骨发育不良患者的互助小组帮助他们应对挑战，分享与疾病相关的经历。