A rare genetic disease-spondyloepiphyseal dysplasia  

A rare genetic disease-spondyloepiphyseal dysplasia

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作  者:YANG Bo LIN Jin JIN Jin WENG Xi-sheng ZHAO Qing QIU Gui-xing 

机构地区:[1]Department of Orthopaedics, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing 100730, China

出  处:《Chinese Medical Journal》2010年第19期2727-2731,共5页中华医学杂志(英文版)

摘  要:Spondyloepiphyseal dysplasia (SED) comprises a group of hereditary disorders caused by osteochondrodysplasia of the spine and long tubular bones owing to chromosome abnormalities) SED can be divided into two major types, termed SED congenita and SED tarda, according to the time of onset,Spondyloepiphyseal dysplasia (SED) comprises a group of hereditary disorders caused by osteochondrodysplasia of the spine and long tubular bones owing to chromosome abnormalities) SED can be divided into two major types, termed SED congenita and SED tarda, according to the time of onset,

关 键 词:OSTEOCHONDRODYSPLASIAS DIAGNOSIS THERAPY 

分 类 号:S831.5[农业科学—畜牧学] Q78[农业科学—畜牧兽医]

 

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