先天性肾上腺增生症和XYY性腺功能减退症。 - Suppr

Suppr

超能文献

Congenital adrenal hyperplasia and XYY hypogonadism.

作者信息

Abraham R R, Wynn V, Heaton D E

出版信息

J R Soc Med. 1985 Aug;78(8):672-4. doi: 10.1177/014107688507800815.

DOI:10.1177/014107688507800815

PMID:4020801

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1289843/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ada9/1289843/54e1c765076c/jrsocmed00206-0074-a.jpg

相似文献

Congenital adrenal hyperplasia and XYY hypogonadism.先天性肾上腺增生症和XYY性腺功能减退症。

J R Soc Med. 1985 Aug;78(8):672-4. doi: 10.1177/014107688507800815.

Effects of the XYY karyotype in one of two brothers with congenital adrenal hyperplasia.先天性肾上腺皮质增生症两兄弟中一人的XYY核型效应。

Clin Genet. 1972;3(6):490-4. doi: 10.1111/j.1399-0004.1972.tb01486.x.

Deletion of the long arm of the Y chromosome in an adolescent with short stature and hypogonadism.一名身材矮小和性腺功能减退的青少年Y染色体长臂缺失。

J Pediatr Endocrinol Metab. 2001 Jan;14(1):103-6. doi: 10.1515/jpem.2001.14.1.103.

XYY karyotype with severe primary hypogonadism. A case report.伴有严重原发性性腺功能减退的XYY核型。病例报告。

J Med Assoc Thai. 1982 May;65(5):277-82.

Hypogonadotropic hypogonadism; the genetic defect. A hypothesis based on human and animal prototypes.低促性腺激素性性腺功能减退；遗传缺陷。基于人类和动物原型的一种假说。

Horm Res. 1992;37 Suppl 3:62-4. doi: 10.1159/000182403.

Genetic analysis of NR0B1 in congenital adrenal hypoplasia patients: identification of a rare regulatory variant resulting in congenital adrenal hypoplasia and hypogonadal hypogonadism without testicular carcinoma in situ.NR0B1 基因在先天性肾上腺发育不全患者中的遗传分析：鉴定一种罕见的调控变异导致先天性肾上腺发育不全和低促性腺激素性性腺功能减退症，而无睾丸原位癌。

Sex Dev. 2012;6(6):284-91. doi: 10.1159/000342295. Epub 2012 Sep 27.

XYY syndrome and acute myeloblastic leukemia.XYY综合征与急性髓细胞白血病。

Cancer Genet Cytogenet. 1987 Feb;24(2):363-5. doi: 10.1016/0165-4608(87)90120-8.

A microdeletion within DAX-1 in X-linked adrenal hypoplasia congenita and hypogonadotrophic hypogonadism.X连锁先天性肾上腺发育不全和低促性腺激素性性腺功能减退中DAX-1基因内的微缺失。

J Investig Med. 1999 May;47(5):232-5.

Sexual infantilism related to adrenogenital syndrome in conjunction with a chromosomal defect.与肾上腺性征异常综合征相关并伴有染色体缺陷的性幼稚症。

Am J Obstet Gynecol. 1977 Dec 15;129(8):919-20. doi: 10.1016/0002-9378(77)90527-0.

Triple-x syndrome accompanied by congenital adrenal hyperplasia: case report.伴有先天性肾上腺增生的XXX综合征：病例报告

Turk J Pediatr. 2004 Oct-Dec;46(4):377-9.

引用本文的文献

Gonadal function in patients with 47,XYY syndrome: a systematic review and meta-analysis.47,XYY综合征患者的性腺功能：系统评价与荟萃分析

Endocr Connect. 2025 Mar 4;14(4). doi: 10.1530/EC-24-0697. Print 2025 Apr 1.

本文引用的文献

The occurrence and significance of Leydig cell proliferation in familial adrenal cortical hyperplasia.家族性肾上腺皮质增生中睾丸间质细胞增殖的发生及意义

J Clin Endocrinol Metab. 1951 Dec;11(12):1436-53. doi: 10.1210/jcem-11-12-1436.

The testis. V. Use of testicular biopsies in the differential diagnosis of precocious puberty.睾丸。五、睾丸活检在性早熟鉴别诊断中的应用。

Pediatrics. 1951 Nov;8(5):701-16.

The testis. III. Absence of germ cells; sclerosing tubular degeneration; "male climacteric".睾丸。III. 生殖细胞缺失；硬化性小管变性；“男性更年期”

AMA Arch Pathol. 1951 Mar;51(3):293-311.

The prepubertal testicular lesion in chromatin-positive Klinefelter's syndrome (primary micro-orchidism) as seen in mentally handicapped children.在智力障碍儿童中所见的染色质阳性克兰费尔特综合征（原发性小睾丸症）的青春期前睾丸病变。

Lancet. 1959 Jan 31;1(7066):219-22. doi: 10.1016/s0140-6736(59)90049-2.

Spermatogenic maturation arrest and the male adrenogenital syndrome.精子发生成熟停滞与男性肾上腺生殖综合征。

Lancet. 1958 Oct 25;2(7052):904-5. doi: 10.1016/s0140-6736(58)92335-3.

Further studies on the treatment of congenital adrenal hyperplasia with cortisone. V. Effects of cortisone therapy on testicular development.关于用可的松治疗先天性肾上腺皮质增生的进一步研究。五、可的松疗法对睾丸发育的影响。

J Clin Endocrinol Metab. 1954 Mar;14(3):287-96. doi: 10.1210/jcem-14-3-287.

XYY karyotype in a case of familial hypogonadism.家族性性腺功能减退病例中的XYY核型

J Clin Endocrinol Metab. 1966 Apr;26(4):443-52. doi: 10.1210/jcem-26-4-443.

The "YY syndrome".“YY综合征”。

Med J Aust. 1969 Aug 30;2(9):443-6. doi: 10.5694/j.1326-5377.1969.tb107190.x.

Pathologic testicular findings in Klinefelter's syndrome. 47,XXY vs 46,XY-47,XXY.克兰费尔特综合征的睾丸病理表现。47,XXY与46,XY - 47,XXY对比

Arch Intern Med. 1972 Nov;130(5):726-9.

Klinefelter's syndrome and its variants: a hormonal and chromosomal study.克兰费尔特综合征及其变异型：一项激素与染色体研究。

Recent Prog Horm Res. 1968;24:321-63. doi: 10.1016/b978-1-4831-9827-9.50013-7.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验