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Variable expression in a dominantly inherited skeletal dysplasia with similarities to brachydactyly E and spondyloepiphyseal-spondyloperipheral dysplasia.

作者信息

Sybert V P, Byers P H, Hall J G

出版信息

Clin Genet. 1979 Feb;15(2):160-6. doi: 10.1111/j.1399-0004.1979.tb01755.x.

DOI:10.1111/j.1399-0004.1979.tb01755.x
PMID:104811
Abstract

Variable expression and penetrance of dominantly inherited disorders present problems in diagnosis and counseling. The variation in clinical findings within a family with an autosomal dominant skeletal dysplasia is presented. In some members only shortened metacarpals were found, as seen in classic Brachydactyly E. Others presented with more severe and generalized skeletal involvement, such as is found in some of the spondyloepiphyseal dysplasias. This family may represent the true spectrum of Brachydactyly E; they may be affected with a specific spondyloepiphyseal dysplasia; or they may represent a new syndrome. The authors favor the first possibility and feel that this family serves to emphasize the importance of examining all affected members in a kindred with an autosomal dominant disease.

摘要

相似文献

1
Variable expression in a dominantly inherited skeletal dysplasia with similarities to brachydactyly E and spondyloepiphyseal-spondyloperipheral dysplasia.
Clin Genet. 1979 Feb;15(2):160-6. doi: 10.1111/j.1399-0004.1979.tb01755.x.
2
Spondyloepiphyseal dysplasia.脊椎骨骺发育不良
J Med Genet. 1983 Apr;20(2):117-21.
3
New skeletal dysplasia with unique brachydactyly.
Am J Med Genet. 1992 Mar 1;42(5):706-13. doi: 10.1002/ajmg.1320420516.
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Birth Defects Orig Artic Ser. 1977;13(3B):149-65.
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Unclassified short stature, possibly spondyloepiphyseal dysplasia, possibly multiple epiphyseal dysplasia, in father and daughter.未分类的身材矮小,父亲和女儿可能患有脊椎骨骺发育不良,也可能患有多发性骨骺发育不良。
Birth Defects Orig Artic Ser. 1974;10(12):399-405.
6
Hereditary brachydactyly with nail dysplasia.伴有指甲发育异常的遗传性短指畸形。
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7
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引用本文的文献

1
Spondyloepiphyseal dysplasia and precocious osteoarthritis in a family with an Arg75-->Cys mutation in the procollagen type II gene (COL2A1).一个家族中因II型前胶原基因(COL2A1)发生精氨酸75突变为半胱氨酸而导致脊椎骨骺发育不良和早发性骨关节炎。
Hum Genet. 1993 Nov;92(5):499-505. doi: 10.1007/BF00216458.
2
Spondyloepiphyseal dysplasia.脊椎骨骺发育不良
J Med Genet. 1983 Apr;20(2):117-21.