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两兄弟患索托斯综合征。

Sotos syndrome in two brothers.

作者信息

Boman H, Nilsson D

出版信息

Clin Genet. 1980 Dec;18(6):421-7. doi: 10.1111/j.1399-0004.1980.tb01787.x.

Abstract

Two brothers presented from birth with features characteristic of Sotos syndrome (cerebral gigantism): overgrowth, craniofacial abnormalities, and mental retardation with hyperactive and aggressive behavior. X-ray examination of the hands revealed imbalanced and advanced skeletal age in one, whereas anterior fontanel bones were present in both brothers. Various hormone concentrations in plasma were all within normal limits, as were the results of a search for abnormal metabolites in plasma and urine. The occurrence of this usually sporadic syndrome in two sons of possible remotely consanguineous, healthy parents, suggests that in some cases Sotos syndrome may be inherited as an autosomal recessive trait. Thus our observation may support the suggestion of heterogeneity of Sotos syndrome. Until specific tests for the identification of various types are available, genetic counseling for this syndrome is difficult.

摘要

两兄弟自出生起就表现出索托斯综合征(脑性巨人症)的特征:生长过速、颅面异常、智力迟钝伴多动和攻击性行为。手部X线检查显示其中一人骨骼年龄失衡且超前,而两兄弟的前囟骨均存在。血浆中各种激素浓度均在正常范围内,血浆和尿液中异常代谢物的检测结果也正常。这种通常为散发性的综合征出现在可能有远亲关系的健康父母的两个儿子身上,表明在某些情况下,索托斯综合征可能作为常染色体隐性性状遗传。因此,我们的观察结果可能支持索托斯综合征具有异质性的观点。在有针对不同类型的特异性检测方法之前,对该综合征进行遗传咨询很困难。

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