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自身免疫性多内分泌腺病–念珠菌病–外胚层营养不良(APECED):常染色体隐性遗传。

Autoimmune polyendocrinopathy--candidosis--ectodermal dystrophy (APECED): autosomal recessive inheritance.

作者信息

Ahonen P

出版信息

Clin Genet. 1985 Jun;27(6):535-42. doi: 10.1111/j.1399-0004.1985.tb02037.x.

Abstract

A genetic analysis was made of 58 patients and their 42 families with APECED (autoimmune polyendocrinopathy--candidosis--ectodermal dystrophy). APECED is characterized by hypoparathyroidism, primary adrenocortical failure and chronic mucocutaneous candidosis, but none of its components is constant. Other endocrine deficiencies can occur as well and also dystrophy of dental enamel and nails. The proportion of affected siblings was 0.147 +/- 0.034 (S.D.) when corrected for truncate single ascertainment, 0.246 +/- 0.019 when corrected for a priori truncate complete ascertainment and 0.240 +/- 0.047 when corrected for a posteriori truncate complete ascertainment. The male/female ratio was 1.04. The results are compatible with autosomal recessive transmission. No heterozygous manifestations of the gene were found. The gene is enriched in isolated subpopulations in central and eastern Finland. APECED is part of the "Finnish heritage of disease".

摘要

对58例自身免疫性多内分泌腺病-念珠菌病-外胚层营养不良(APECED)患者及其42个家系进行了基因分析。APECED的特征为甲状旁腺功能减退、原发性肾上腺皮质功能衰竭和慢性黏膜皮肤念珠菌病,但其任何一个组成部分都并非一成不变。也可能出现其他内分泌缺陷以及牙釉质和指甲营养不良。校正截短单例确诊后,受累同胞的比例为0.147±0.034(标准差),校正先验截短完全确诊后为0.246±0.019,校正后验截短完全确诊后为0.240±0.047。男女比例为1.04。结果符合常染色体隐性遗传。未发现该基因的杂合表现。该基因在芬兰中部和东部的孤立亚群中富集。APECED是“芬兰疾病遗传”的一部分。

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