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马来西亚儿童X连锁无丙种球蛋白血症的临床模式

Clinical patterns of X linked agammaglobulinemia in Malaysian children.

作者信息

Noh L M, Ismail Z, Zainudin B M, Low S M, Azizi B H, Noah R M, Nasaruddin B A

机构信息

Department of Immunology, Universiti Sains Malaysia Kelantan, Kuala Lumpur, Malaysia.

出版信息

Acta Paediatr Jpn. 1995 Jun;37(3):331-5. doi: 10.1111/j.1442-200x.1995.tb03324.x.

Abstract

X linked agammaglobulinemia (XLA) is rarely reported from developing countries especially from South East Asia. It appears that X linked agammaglobulinemia is less common in certain ethnic groups. It is very uncommon in black people in USA and South Africa. In multiracial Malaysia we have documented five XLA in Malays and Indians but not in the Chinese that constitute about 31% of the population. First degree relatives afflicted with XLA or other primary immunodeficiencies occurred more often in our study. All showed lung involvement although the etiologic organisms involved were atypical, being Gram negative.

摘要

X连锁无丙种球蛋白血症(XLA)在发展中国家鲜有报道,尤其是在东南亚地区。似乎X连锁无丙种球蛋白血症在某些种族群体中不太常见。在美国和南非的黑人中非常罕见。在多民族的马来西亚,我们记录了5例马来人和印度人的XLA病例,但在占人口约31%的华人中未发现。在我们的研究中,患XLA或其他原发性免疫缺陷的一级亲属更为常见。所有病例均有肺部受累,尽管所涉及的病原体不典型,为革兰氏阴性菌。

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