Spondylocarpotarsal synostosis syndrome. A rare case of short stature and congenital scoliosis.

Q3 Medicine Clinical Cases in Mineral and Bone Metabolism Pub Date : 2017-05-01 Epub Date: 2017-10-25 DOI:10.11138/ccmbm/2017.14.2.258
Swayamsidha Mangaraj, Arun Kumar Choudhury, Mamata Singh, Debasish Patro, Anoj Kumar Baliarsinha
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引用次数: 3

Abstract

Spondylocarpotarsal synostosis is a very rare skeletal disorder characterized by vertebral malsegmentation defects. Apart from severe vertebral defects, the disease is associated with carpal and tarsal synostosis which is quite characteristic for the disease. We report a case of young child who presented with short stature and congenital scoliosis. The radiological and clinical findings were compatible with the above diagnosis. Apart from the classical findings, the patient had evidence of odontoid aplasia which has not earlier been described in association with this disorder. We report this case for rarity of this disorder and the associated novel finding.

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峡部枢椎关节闭锁综合征。一个罕见的矮小和先天性脊柱侧凸的病例。
峡部峡部关节闭锁是一种非常罕见的骨骼疾病,其特征是椎体分割不良。除了严重的椎体缺损外,该病还伴有腕关节和跗骨关节闭锁,这是该病的典型特征。我们报告一个年轻的孩子谁提出了矮小的身材和先天性脊柱侧凸的情况。放射学和临床表现符合上述诊断。除了经典的发现,患者有证据表明齿状体发育不全,以前没有描述过与这种疾病有关。我们报告这个病例的罕见性和相关的新发现。
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来源期刊
Clinical Cases in Mineral and Bone Metabolism
Clinical Cases in Mineral and Bone Metabolism ENDOCRINOLOGY & METABOLISM-
CiteScore
2.60
自引率
0.00%
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0
期刊介绍: The Journal encourages the submission of case reports and clinical vignettes that provide new and exciting insights into the pathophysiology and characteristics of disorders related to skeletal function and mineral metabolism and/or highlight pratical diagnostic and /or therapeutic considerations.
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