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Additional evidence of gradual loss of germ cells in the pathogenesis of streak ovaries in Turner's syndrome.

作者信息

Weiss L

出版信息

J Med Genet. 1971 Dec;8(4):540-4. doi: 10.1136/jmg.8.4.540.

DOI:10.1136/jmg.8.4.540
PMID:5149541
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1469104/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e66/1469104/a5931981ec2e/jmedgene00367-0147-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e66/1469104/f39af231edd1/jmedgene00367-0145-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e66/1469104/5e206e2cb9ca/jmedgene00367-0146-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e66/1469104/a5931981ec2e/jmedgene00367-0147-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e66/1469104/f39af231edd1/jmedgene00367-0145-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e66/1469104/5e206e2cb9ca/jmedgene00367-0146-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e66/1469104/a5931981ec2e/jmedgene00367-0147-a.jpg

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Additional evidence of gradual loss of germ cells in the pathogenesis of streak ovaries in Turner's syndrome.特纳综合征中条索状卵巢发病机制中生殖细胞逐渐丢失的更多证据。
J Med Genet. 1971 Dec;8(4):540-4. doi: 10.1136/jmg.8.4.540.
2
Somatic stigmata of Turner's syndrome in a patient with 46,XXq-.一名核型为46,XXq-的患者的特纳综合征躯体体征
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A dicentric Y chromosome without evidence of sex chromosomal mosaicism, 46,XYqdic, in a patient with features of Turner's syndrome.一名患有特纳综合征特征的患者，其Y染色体呈双着丝粒，无性染色体嵌合现象，核型为46,XYq dic。
J Med Genet. 1972 Mar;9(1):96-100. doi: 10.1136/jmg.9.1.96.
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Evidence for X-X chromosome translocation in humans.人类X染色体与X染色体易位的证据。
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[A CASE OF BONNEVIE-ULRICH-TURNER SYNDROME WITH GONADAL DYSGENESIS AND KARYOTYPE 45/XO].[一例性腺发育不全且核型为45,XO的邦纳维-乌尔里希-特纳综合征病例]
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Shear wave elastography to assess stiffness of the human ovary and other reproductive tissues across the reproductive lifespan in health and disease†.剪切波弹性成像评估健康和疾病状态下人类卵巢和其他生殖组织在整个生殖寿命周期中的硬度。
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International consensus: ovarian tissue cryopreservation in young Turner syndrome patients: outcomes of an ethical Delphi study including 55 experts from 16 different countries.

本文引用的文献

1
GONADAL DYSGENESIS IN A WOMAN AFTER SEVENTEEN YEARS OF REGULAR MENSES.一名有规律月经17年后出现性腺发育不全的女性。
Am J Obstet Gynecol. 1965 Jan 1;91:106-9. doi: 10.1016/0002-9378(65)90594-6.
2
THE PATHOLOGY AND CYTOGENETICS OF GONADAL AGENESIS.
Am J Obstet Gynecol. 1963 Nov 1;87:578-600. doi: 10.1016/0002-9378(63)90051-6.
3
45/XO Turner's syndrome in the newborn: report of two cases.新生儿45/XO特纳综合征：两例报告。
J Clin Endocrinol Metab. 1963 Jan;23:1-10. doi: 10.1210/jcem-23-1-1.
国际共识：年轻特纳综合征患者卵巢组织冷冻保存：一项伦理德尔菲研究的结果，该研究包括来自 16 个不同国家的 55 名专家。
Hum Reprod. 2020 May 1;35(5):1061-1072. doi: 10.1093/humrep/deaa007.
4
TurnerFertility trial: PROTOCOL for an observational cohort study to describe the efficacy of ovarian tissue cryopreservation for fertility preservation in females with Turner syndrome.特纳生育力试验：一项观察性队列研究的方案，旨在描述卵巢组织冷冻保存对特纳综合征女性生育力保存的疗效。
BMJ Open. 2019 Dec 11;9(12):e030855. doi: 10.1136/bmjopen-2019-030855.
5
Depression in Turner Syndrome: A Systematic Review.特纳综合征中的抑郁：系统综述。
Arch Sex Behav. 2020 Feb;49(2):769-786. doi: 10.1007/s10508-019-01549-1. Epub 2019 Oct 9.
6
Fertility counseling and preservation discussions for females with Turner syndrome in pediatric centers: practice patterns and predictors.特纳综合征女性的生育咨询和保存讨论：儿科中心的实践模式和预测因素。
Fertil Steril. 2019 Oct;112(4):740-748. doi: 10.1016/j.fertnstert.2019.05.010. Epub 2019 Jul 1.
7
Outcomes of spontaneous and assisted pregnancies in Turner syndrome: the U.S. National Institutes of Health experience.特纳综合征患者自发性妊娠和辅助妊娠的结局：美国国立卫生研究院的经验。
Fertil Steril. 2011 Jun;95(7):2251-6. doi: 10.1016/j.fertnstert.2011.03.085. Epub 2011 Apr 15.
8
Normal US appearance of ovaries and uterus in four patients with Turner's syndrome and 45,X karyotype.4例特纳综合征且核型为45,X的患者卵巢和子宫的超声表现正常。
Pediatr Radiol. 1996;26(1):37-9. doi: 10.1007/BF01403702.
9
Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features.特纳综合征与女性性染色体畸变：推导临床特征发展中涉及的主要因素。
Hum Genet. 1995 Jun;95(6):607-29. doi: 10.1007/BF00209476.
10
Gonadal function in galactosemics and in galactose-intoxicated animals.半乳糖血症患者及半乳糖中毒动物的性腺功能。
Eur J Pediatr. 1995;154(7 Suppl 2):S14-20. doi: 10.1007/BF02143797.
4
Gonadal dysgenesis: the genetic significance of unusual variants.
Acta Endocrinol (Copenh). 1960 Jan;33:89-102. doi: 10.1530/acta.0.xxxiii0089.
5
Klinefelter's syndrome in a ten-month-old mongolian idiot: report of a case with chromosome analysis.
N Engl J Med. 1960 Nov 3;263:887-90. doi: 10.1056/NEJM196011032631804.
6
[Turner syndrome with fully developed secondary sex characteristics and fertility].具有完全发育的第二性征和生育能力的特纳综合征
Acta Endocrinol (Copenh). 1960 Nov;35:397-404.
7
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.
8
The anatomy and histology of XO human embryos and fetuses.
Anat Rec. 1966 Jul;155(3):369-83. doi: 10.1002/ar.1091550309.
9
[Ullrichturner syndrome in the newborn associated with coarctation of the aorta and left-sided superior vena cava].新生儿Ullrich-Turner综合征合并主动脉缩窄及左侧上腔静脉
Ann Paediatr. 1965;204(6):387-96.
10
Germ cells in the ovaries of XO female infants.
Am J Clin Pathol. 1968 Apr;49(4):521-6. doi: 10.1093/ajcp/49.4.521.