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Léri's pleonosteosis.

作者信息

Hilton R C, Wentzel J

出版信息

Q J Med. 1980 Autumn;49(196):419-29.

PMID:6791240
Abstract

Seven members of one family with Léri's pleonosteosis are reported. The abnormalities found provide further clarification of the clinical features of this rare inherited disorder. There was no evidence of genetic linkage between Léri's pleonosteosis and various parameters measured. We draw attention to the importance of recognizing this and similar rare inherited dystrophies, since the prognosis is good and inappropriate therapy should be avoided.

摘要

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Léri's pleonosteosis.
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[Tribute to André Léri. Clinical, radiologic and anatomic study of the first case of pleonosteosis].[向安德烈·勒里致敬。多指(趾)畸形首例病例的临床、放射学及解剖学研究]
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Heritable disorders of connective tissue. VIII. Concluding comments. Introduction; fibrodysplasia ossificans progressiva; osteopoikilosis; Leri's pleonosteosis; Paget's disease of bone; other possible hereditary and generalized disorders of connective tissue; the future in the study of heritable disorders of connective tissue; general summary and conclusions.结缔组织遗传性疾病。VIII. 总结评论。引言;进行性骨化性纤维发育不良;骨斑点症;勒里氏骨肥厚症;佩吉特骨病;其他可能的遗传性全身性结缔组织疾病;结缔组织遗传性疾病研究的未来;总体总结与结论。
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