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特纳综合征患者及其亲属的人类白细胞抗原频率、糖尿病和自身免疫性

HLA frequencies, diabetes mellitus and autoimmunity in Turner's patients and their relatives.

作者信息

Cassidy S B, Niblack G D, Lorber C A, Mann J M, Engel E

出版信息

Ann Genet. 1978 Dec;21(4):203-8.

PMID:314255
Abstract

In a preliminary study of twenty-three patients with gonadal dysgenesis (Turner's syndrome) and their families, correlation was sought between their serum defined HLA allele frequencies and their known tendencies toward abnormal immune responses and diabetes mellitus, since individuals with the latter disorders have been shown to have an increased frequency of certain HLA types. We were unable to demonstrate an association between these major serum-defined histocompatibility antigens, immune homeostasis disturbances and sex chromosome aneuploidy in this group. It is felt, however, that testing involving the patterns of HLA-D and "HLA-D related" antigen frequencies should be obtained to further evaluate the possibility of such an association.

摘要

在一项对23例性腺发育不全(特纳综合征)患者及其家族的初步研究中,鉴于已表明患有免疫反应异常和糖尿病的个体中某些HLA类型的频率增加,因此研究了他们血清中确定的HLA等位基因频率与已知的异常免疫反应倾向和糖尿病倾向之间的相关性。在该组中,我们未能证明这些主要血清定义的组织相容性抗原、免疫稳态紊乱和性染色体非整倍体之间存在关联。然而,有人认为,应该进行涉及HLA-D和“与HLA-D相关”抗原频率模式的检测,以进一步评估这种关联的可能性。

相似文献

1
HLA frequencies, diabetes mellitus and autoimmunity in Turner's patients and their relatives.特纳综合征患者及其亲属的人类白细胞抗原频率、糖尿病和自身免疫性
Ann Genet. 1978 Dec;21(4):203-8.
2
Parental segregation of autoimmunity in patients with Turner's syndrome: preferential paternal transmission?特纳综合征患者自身免疫性疾病的亲代遗传:父系优先传递?
J Autoimmun. 1999 Feb;12(1):65-72. doi: 10.1006/jaut.1998.0250.
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Halo nevus, rather than vitiligo, is a typical dermatologic finding of turner's syndrome: clinical, genetic, and immunogenetic study in 72 patients.晕痣而非白癜风是特纳综合征典型的皮肤表现:72例患者的临床、遗传学及免疫遗传学研究
J Am Acad Dermatol. 2004 Sep;51(3):354-8. doi: 10.1016/j.jaad.2003.11.082.
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Adrenocorticotrophin stimulation and HLA polymorphisms suggest a high frequency of heterozygosity for steroid 21-hydroxylase deficiency in patients with Turner's syndrome and their families.促肾上腺皮质激素刺激试验和人类白细胞抗原多态性表明,特纳综合征患者及其家族中类固醇21-羟化酶缺乏症的杂合子频率较高。
Clin Endocrinol (Oxf). 1994 Jan;40(1):39-45. doi: 10.1111/j.1365-2265.1994.tb02441.x.
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Autoimmunity, HLA, Gm and Km polymorphisms in Turner's syndrome.特纳综合征中的自身免疫、HLA、Gm和Km多态性
Autoimmunity. 1989;4(1-2):69-78. doi: 10.3109/08916938909034361.
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[Thyroiditis and Turner's syndrome].[甲状腺炎与特纳综合征]
Arch Fr Pediatr. 1988 Jun-Jul;45(6):411-2.
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Diabetes mellitus and thyroid autoimmunity in gonadal dysgenesis.
Fertil Steril. 1973 Jan;24(1):1-9. doi: 10.1016/s0015-0282(16)39428-6.
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Endocrine, cytogenetic and psychometric features of patients with X-isochromosome 46, X, i(Xq) Turner's syndrome: a preliminary study in nine patients.
Clin Invest Med. 1984;7(3):135-41.
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[Diabetes mellitus type I, thyroid gland autoimmunity, thyroid gland function and HLA status].[1型糖尿病、甲状腺自身免疫、甲状腺功能及人类白细胞抗原状态]
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[45, XO Turner's syndrome associated with menarche and diabetes mellitus].
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Hyperglycemia in Turner syndrome: Impact, mechanisms, and areas for future research.特纳综合征中的高血糖症:影响、机制和未来研究领域。
Front Endocrinol (Lausanne). 2023 Feb 15;14:1116889. doi: 10.3389/fendo.2023.1116889. eCollection 2023.
2
Reduced secretion of gastric inhibitory polypeptide in Turner patients with impaired glucose tolerance.
Eur J Pediatr. 1991 Mar;150(5):339-42. doi: 10.1007/BF01955936.