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迪格维-梅尔基奥尔-克劳森侏儒症的异质性。

Heterogeneity of Dyggve-Melchior-Clausen dwarfism.

作者信息

Spranger J, Bierbaum B, Herrmann J

出版信息

Hum Genet. 1976 Aug 30;33(3):279-87. doi: 10.1007/BF00286853.

Abstract

Sibs with apparent Dyggve-Melchior-Clausen (DMC) dwarfism and normal intelligence are described. Three other familial and 3 sporadic cases with DMC dwarfism and normal intelligence are known. Twelve familial and 9 sporadic cases are known with the usual combination of DMC dwarfism and severe mental retardation. Since the two conditions appear to breed true they seem to be genetically different. We propose to name the former "Smith-McCort dwarfism" to clearly distinguish it from the DMC syndrome in which mental retardation is a constituent part. Both conditions are inherited as autosomal recessive traits. Spinal cord compression due to atlantoaxial instability is a serious and preventable complication of both disorders.

摘要

本文描述了患有明显的迪格维-梅尔基奥尔-克劳森(DMC)侏儒症且智力正常的同胞兄弟姐妹。另外已知还有3例家族性和3例散发性DMC侏儒症且智力正常的病例。已知有12例家族性和9例散发性病例患有常见的DMC侏儒症并伴有严重智力迟钝。由于这两种情况似乎都能真实遗传,它们在遗传上似乎是不同的。我们建议将前者命名为“史密斯-麦科特侏儒症”,以明确将其与智力迟钝作为组成部分的DMC综合征区分开来。这两种情况均作为常染色体隐性性状遗传。寰枢椎不稳定导致的脊髓压迫是这两种疾病严重且可预防的并发症。

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