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首页> 外文期刊>Clinical Genetics: An International Journal of Genetics in Medicine >Split hand/foot malformation with long-bone deficiency and BHLHA9 duplication: Report of 13 new families
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Split hand/foot malformation with long-bone deficiency and BHLHA9 duplication: Report of 13 new families

机译:手足畸形合并长骨缺乏症和BHLHA9重复:13个新家庭的报告

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摘要

Split hand/foot malformation (SHFM) with long-bone deficiency (SHFLD, MIM#119100) is a rare condition characterized by SHFM associated with long-bone malformation usually involving the tibia. Previous published data reported several unrelated patients with 17p13.3 duplication and SHFLD. Recently, the minimal critical region had been reduced, suggesting that BHLHA9 copy number gains are associated with this limb defect. Here, we report on 13 new families presenting with ectrodactyly and harboring a BHLHA9 duplication.
机译:伴有长骨缺乏症的手脚分离畸形(SHFM)(SHFLD,MIM#119100)是一种罕见的疾病,其特征在于SHFM与通常涉及胫骨的长骨畸形相关。先前发表的数据报道了几例无关的17p13.3重复和SHFLD患者。最近,最小的临界区已经减少,这表明BHLHA9拷贝数的增加与该肢体缺陷有关。在这里,我们报告13个新的家庭与ectectactyly和包含BHLHA9重复。

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