has acromelia
患有肢端过短症
with acromelia
伴有肢端过短症
acromelia patients
肢端过短症患者
acromelia syndrome
肢端过短综合征
acromelia disorder
肢端过短疾病
acromelia type
肢端过短类型
acromelia case
肢端过短症病例
acromelia diagnosis
肢端过短症诊断
acromelia condition
肢端过短病症
acromelia is a rare genetic condition that leads to disproportionate shortening of the limbs.
肢端发育不全是一种罕见的遗传性疾病，导致四肢不成比例的短缩。
patients with acromelia often experience limited range of motion in their hands and feet.
肢端发育不全患者通常会出现手部和足部活动受限的情况。
the diagnosis of acromelia is typically confirmed through radiographic imaging and genetic testing.
肢端发育不全的诊断通常通过影像学检查和基因检测来确认。
acromelia can be inherited in an autosomal recessive pattern, though sporadic cases also occur.
肢端发育不全可能以常染色体隐性方式遗传，但也存在偶发病例。
early intervention for acromelia includes physical therapy and orthopedic monitoring to improve mobility.
肢端发育不全的早期干预包括物理治疗和骨科监测，以改善活动能力。
researchers are investigating targeted therapies to stimulate growth in individuals with acromelia.
研究人员正在研究针对肢端发育不全个体的靶向疗法，以刺激生长。
support groups provide valuable resources for families coping with the challenges of acromelia.
支持团体为应对肢端发育不全挑战的家庭提供宝贵的资源。
acromelia differs from other forms of dwarfism by primarily affecting the distal portions of limbs.
肢端发育不全与其他形式的侏儒症不同，主要影响四肢的远端部分。
clinical trials are exploring the efficacy of growth hormone treatment for children with acromelia.
临床试验正在探索生长激素治疗对肢端发育不全儿童的疗效。
physicians recommend regular orthopedic assessments for patients diagnosed with acromelia to address complications.
医生建议对诊断为肢端发育不全的患者定期进行骨科评估，以处理并发症。
the psychosocial impact of acromelia can be significant, necessitating psychological counseling and community support.
肢端发育不全的心理社会影响可能很大，需要心理咨询和社区支持。
has acromelia
患有肢端过短症
with acromelia
伴有肢端过短症
acromelia patients
肢端过短症患者
acromelia syndrome
肢端过短综合征
acromelia disorder
肢端过短疾病
acromelia type
肢端过短类型
acromelia case
肢端过短症病例
acromelia diagnosis
肢端过短症诊断
acromelia condition
肢端过短病症
acromelia is a rare genetic condition that leads to disproportionate shortening of the limbs.
肢端发育不全是一种罕见的遗传性疾病，导致四肢不成比例的短缩。
patients with acromelia often experience limited range of motion in their hands and feet.
肢端发育不全患者通常会出现手部和足部活动受限的情况。
the diagnosis of acromelia is typically confirmed through radiographic imaging and genetic testing.
肢端发育不全的诊断通常通过影像学检查和基因检测来确认。
acromelia can be inherited in an autosomal recessive pattern, though sporadic cases also occur.
肢端发育不全可能以常染色体隐性方式遗传，但也存在偶发病例。
early intervention for acromelia includes physical therapy and orthopedic monitoring to improve mobility.
肢端发育不全的早期干预包括物理治疗和骨科监测，以改善活动能力。
researchers are investigating targeted therapies to stimulate growth in individuals with acromelia.
研究人员正在研究针对肢端发育不全个体的靶向疗法，以刺激生长。
support groups provide valuable resources for families coping with the challenges of acromelia.
支持团体为应对肢端发育不全挑战的家庭提供宝贵的资源。
acromelia differs from other forms of dwarfism by primarily affecting the distal portions of limbs.
肢端发育不全与其他形式的侏儒症不同，主要影响四肢的远端部分。
clinical trials are exploring the efficacy of growth hormone treatment for children with acromelia.
临床试验正在探索生长激素治疗对肢端发育不全儿童的疗效。
physicians recommend regular orthopedic assessments for patients diagnosed with acromelia to address complications.
医生建议对诊断为肢端发育不全的患者定期进行骨科评估，以处理并发症。
the psychosocial impact of acromelia can be significant, necessitating psychological counseling and community support.
肢端发育不全的心理社会影响可能很大，需要心理咨询和社区支持。
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