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小头畸形、特殊面容、关节异常及白细胞趋化功能缺陷:Say等人综合征的又一例病例

Microcephaly, characteristic facies, joint abnormalities, and deficient leucocyte chemotaxis: a further case of the syndrome of Say et al.

作者信息

Perandones C, Cerretini R I, Vargas Vera R M, Aranda E I, Alba L G, Pivetta O H

机构信息

Instituto Nacional de Genética Médica, Buenos Aires, Argentina.

出版信息

J Med Genet. 1996 Mar;33(3):227-9. doi: 10.1136/jmg.33.3.227.

Abstract

We report on a 13 year old boy with microcephaly, sloping forehead, prominent nose, scoliosis, and flexion contractures involving the elbows and knees. The patient showed severe mental and growth retardation. Since birth and up to the present he has suffered from multiple and varied infections. Immunological studies showed a marked decrease in leucocyte chemotaxis. Clinical and laboratory findings confirm the similarity of this case to the two brothers described by Say et al. We have not found any descriptions of similar patients. The purpose of this paper is to contribute to the phenotypic delineation of this syndrome and to highlight the need for immunological investigation in patients with multiple congenital malformations.

摘要

我们报告了一名13岁男孩,他患有小头畸形、前额倾斜、鼻子突出、脊柱侧弯以及肘部和膝盖的屈曲挛缩。该患者表现出严重的智力和生长发育迟缓。自出生以来直至目前,他一直遭受多种不同的感染。免疫学研究显示白细胞趋化性显著降低。临床和实验室检查结果证实了该病例与Say等人描述的两兄弟相似。我们尚未发现类似患者的任何描述。本文的目的是为该综合征的表型描述做出贡献,并强调对患有多种先天性畸形的患者进行免疫学调查的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d10/1051873/f833f5f6ffc0/jmedgene00257-0051-a.jpg

相似文献

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The syndrome of Hirschsprung disease, microcephaly, unusual face, and mental retardation.
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