oligospermia

出典: meddic

redirect 乏精子症

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「insufficient spermatozoa in the semen」

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出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2015/06/15 09:55:38」(JST)

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英文文献

  • Minichromosome maintenance complex component 8 (MCM8) gene mutations result in primary gonadal failure.
  • Tenenbaum-Rakover Y1, Weinberg-Shukron A2, Renbaum P3, Lobel O2, Eideh H4, Gulsuner S5, Dahary D6, Abu-Rayyan A7, Kanaan M7, Levy-Lahad E2, Bercovich D8, Zangen D9.
  • Journal of medical genetics.J Med Genet.2015 Jun;52(6):391-9. doi: 10.1136/jmedgenet-2014-102921. Epub 2015 Apr 14.
  • BACKGROUND: Primary gonadal failure is characterised by primary amenorrhoea or early menopause in females, and oligospermia or azoospermia in males. Variants of the minichromosome maintenance complex component 8 gene (MCM8) have recently been shown to be significantly associated with women's menopau
  • PMID 25873734
  • Re: Enclomiphene Citrate Stimulates Testosterone Production while Preventing Oligospermia: A Randomized Phase II Clinical Trial Comparing Topical Testosterone.
  • Niederberger C.
  • The Journal of urology.J Urol.2015 Jun;193(6):2053-5. doi: 10.1016/j.juro.2015.03.052. Epub 2015 Mar 16.
  • PMID 25986825
  • Association of polymorphisms in glutathione S-transferase genes (GSTM1, GSTT1, GSTP1) with idiopathic azoospermia or oligospermia in Sichuan, China.
  • Xiong DK, Chen HH, Ding XP1, Zhang SH, Zhang JH.
  • Asian journal of andrology.Asian J Androl.2015 May-Jun;17(3):481-6. doi: 10.4103/1008-682X.143737.
  • The reported effects of the glutathione S-transferase (GSTs) genes (GSTM1, GSTT1, and GSTP1) on male factor infertility have been inconsistent and even contradictory. Here, we conducted a case-control study to investigate the association between functionally important polymorphisms in GST genes and
  • PMID 25532576

和文文献

  • 診断時にRobertson型転座の先天性染色体異常が判明したフィラデルフィア染色体陽性急性リンパ性白血病
  • 山口 津加彩,五十嵐 愛子,川村 眞智子 [他],小笹 由香,吉田 雅幸,垣花 和彦,坂巻 壽,大橋 一輝
  • 臨床血液 56(5), 481-484, 2015
  • 急性リンパ性白血病(ALL)の40代の男性患者で,精子数の減少と運動率の低下を指摘され,3年ほど前から不妊治療を施行していた。ALL発症時の骨髄染色体検査にて45, XY, t(9;22)(q34;q11.2), der(13;14)(q10;q10)がみられ,フィラデルフィア染色体に加え,13番と14番染色体が融合するRobertson (RT)型転座の存在が判明した。完全寛解到達後の骨髄染色体 …
  • NAID 130005076021
  • 当院におけるTESE及びTESE-ICSIの現況
  • 馬場 聖子,清須 知栄子,徐 東舜,宮川 康,辻村 晃
  • 日本受精着床学会雑誌 27(1), 111-114, 2010-03-20
  • NAID 10027211389
  • Tissue-specific differentially methylated regions of the human VASA gene are potentially associated with maturation arrest phenotype in the testis
  • Sugimoto Kazuhiro,Koh Eitetsu,Sin Ho-Su [他],MAEDA Yuji,NARIMOTO Kazutaka,IZUMI Koji,KOBORI Yoshitomo,KITAMURA Eiko,NAGASE Hiroki,YOSHIDA Atsumi,NAMIKI Mikio
  • Journal of human genetics 54(8), 450-456, 2009-08-01
  • … A total of 131 male patients with idiopathic azoospermia or severe oligospermia were evaluated histologically, and the methylation status of CpG islands in the VASA gene was screened. …
  • NAID 10030731316

関連リンク

Oligospermia defined as less number of sperm in the ejaculate of the male or less than 20 million sperm per milliliter. Normal Sperm count : 20 million / milliliter to 120 million / milliliter Sperm count below 20 million/ml called ...
Oligospermia : Oligospermia defined as less number of sperm in the ejaculate of the male or less than 20 million sperm per milliliter.?/span> Normal Sperm count : 20 million / milliliter?to 120 ...

関連画像

OligospermiaCount Treatment India, Cost Oligospermia  and 9 patients developed oligospermiaSymptoms and indications: Seminal fluid tn_oligospermiaOligospermia Treatment


★リンクテーブル★
先読み乏精子症
リンク元精液過少症」「oligozoospermia」「low sperm count

乏精子症」

  [★]

oligozoospermia, low sperm count
乏精子、精子減少症?、精子欠乏症?、精子過少症
精液検査、無精子症男性不妊症
[show details]
  • 精子濃度20x10^6以下



精液過少症」

  [★]

oligospermia, hypospermia
精液減少症乏精液症乏精液
精子減少症乏精子症精子数減少


oligozoospermia」

  [★]

精子減少症乏精子症精子欠乏症

low sperm countoligospermia


low sperm count」

  [★]

oligospermiaoligozoospermia




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