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A novel mutation in TPRS1 gene caused tricho-rhino-phalangeal syndrome in a Chinese patient with severe osteoporosis 被引量:1
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作者 SHAO Cong TIAN Jun +5 位作者 SHI Dong-hong YU Chun-xiao XU Chao WANG Lai-cheng GAO Ling ZHAO Jia-jun 《Chinese Medical Journal》 SCIE CAS CSCD 2011年第10期1583-1585,共3页
Tricho-rhino-phalangeal syndrome (TRPS) was first reported in 1966. Although mutation of TRPS1 gene is considered to be responsible for the syndromes in 2000, investigation of bone metabolism and changes of serum in... Tricho-rhino-phalangeal syndrome (TRPS) was first reported in 1966. Although mutation of TRPS1 gene is considered to be responsible for the syndromes in 2000, investigation of bone metabolism and changes of serum insulin-like growth factor (IGF)-1 level in this kind of patients is rare. Here, we report a patient with TRPS I (MIM 190350) presenting a novel mutation (1096insA) and abnormal changes of severe osteoporosis as well as low serum IGF-I level. 展开更多
关键词 OSTEOPOROSIS tricho-rhino-phalangeal syndrome TRPS1 gene
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