Literature DB >> 6800930

Meiotic arrest at first spermatocyte level: a new inherited infertility disorder.

J M Cantú, F Rivas, P Hernández-Jáuregui, M Díaz, V Cortés-Gallegos, G Vaca, A Velázquez, B Ibarra.   

Abstract

Three 46,XY phenotypically male, azoospermic brothers out of thirteen sibs from a consanguineous marriage were studied and found to have a unique pattern of testicular histology with arrest of spermatogenesis at the pachytene stage of primary spermatocytes. Endocrinological evaluation showed elevated plasma luteinizing(LH) and normal to elevated follicle-stimulating (FSH) hormones, positive gonadotropin pituitary response to luteinizing hormone-releasing hormone, depletion of LH and FSH levels by exogenous testosterone (T) administration, normal levels of T and dihydrotestosterone hormones, and elevation of T after stimulation with human chorionic gonadotropin hormone. Electrophoretic assay of lactic dehydrogenase isozymes did not reveal band C4 in semen or testicular tissue. These traits seem to constitute a hitherto undescribed form of infertility in which spermatogenesis arrest at the first spermatocyte level is the main feature. The parental consanguinity suggests autosomal recessive inheritance.

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Year:  1981        PMID: 6800930     DOI: 10.1007/BF00295476

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  8 in total

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Authors:  M Hultén; A J Solari; N E Skakkebaek
Journal:  Hereditas       Date:  1974       Impact factor: 3.271

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Journal:  J Reprod Fertil       Date:  1973-10

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Journal:  Rev Invest Clin       Date:  1973 Oct-Dec       Impact factor: 1.451

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Authors:  B Dutrillaux; J Guéguen
Journal:  Ann Genet       Date:  1971-03

6.  Low chiasma count and other meiotic irregularities in two infertile 46, XY men with spermatogenic arrest.

Authors:  M Hultén; R Eliasson; K G Tillinger
Journal:  Hereditas       Date:  1970       Impact factor: 3.271

7.  A gross reduction in chiasma formation during meiotic prophase and a defective DNA repair mechanism associated with a case of human male infertility.

Authors:  P L Pearson; J D Ellis; H J Evans
Journal:  Cytogenetics       Date:  1970

8.  Human male infertility, probably genetically determined, due to defective meiosis and spermatogenic arrest.

Authors:  R S Chaganti; J German
Journal:  Am J Hum Genet       Date:  1979-09       Impact factor: 11.025

  8 in total
  3 in total

1.  Human male infertility associated with mutations in NR5A1 encoding steroidogenic factor 1.

Authors:  Anu Bashamboo; Bruno Ferraz-de-Souza; Diana Lourenço; Lin Lin; Neil J Sebire; Debbie Montjean; Joelle Bignon-Topalovic; Jacqueline Mandelbaum; Jean-Pierre Siffroi; Sophie Christin-Maitre; Uppala Radhakrishna; Hassan Rouba; Celia Ravel; Jacob Seeler; John C Achermann; Ken McElreavey
Journal:  Am J Hum Genet       Date:  2010-10-08       Impact factor: 11.025

2.  Insight into 2,3,7,8-tetrachlorodibenzo-p-dioxin-induced disruption of zebrafish spermatogenesis via single cell RNA-seq.

Authors:  Alex Haimbaugh; Camille Akemann; Danielle Meyer; Katherine Gurdziel; Tracie R Baker
Journal:  PNAS Nexus       Date:  2022-06-22

3.  Human Spermatogenesis: Insights From the Clinical Care of Men With Infertility.

Authors:  Peter N Schlegel
Journal:  Front Endocrinol (Lausanne)       Date:  2022-05-18       Impact factor: 6.055

  3 in total

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