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Phenotypes of Sperm Pathology: Genetic and Acquired Forms in Infertile Men

2000; Wiley; Volume: 21; Issue: 6 Linguagem: Inglês

10.1002/j.1939-4640.2000.tb03409.x

2047-2927

H Chemes,

Reproductive Biology and Fertility

Journal of AndrologyVolume 21, Issue 6 p. 799-808 Free Access Phenotypes of Sperm Pathology: Genetic and Acquired Forms in Infertile Men HECTOR E. CHEMES MD, PhD, Corresponding Author HECTOR E. CHEMES MD, PhD Laboratory of Testicular Physiology and Pathology, Endocrinology Division, Buenos Aires Children's Hospital, Buenos Aires, Argentina (e-mail: [email protected]).Laboratory of Testicular Physiology and Pathology, Endocrinology Division, Buenos Aires Children's Hospital, Buenos Aires, Argentina.Search for more papers by this author HECTOR E. CHEMES MD, PhD, Corresponding Author HECTOR E. CHEMES MD, PhD Laboratory of Testicular Physiology and Pathology, Endocrinology Division, Buenos Aires Children's Hospital, Buenos Aires, Argentina (e-mail: [email protected]).Laboratory of Testicular Physiology and Pathology, Endocrinology Division, Buenos Aires Children's Hospital, Buenos Aires, Argentina.Search for more papers by this author First published: 02 January 2013 https://doi.org/10.1002/j.1939-4640.2000.tb03409.xCitations: 13AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat References Abramsson L., Beckman G., Duchek M., Nordenson I. Chromosomal aberrations and male infertility. J Urol. 1982; 128: 52–53. Acosta AA, Khalifa E., Oehninger S. Pure human follicle stimulating hormone has a role in the treatment of severe male infertility by assisted reproduction: Norfolk's total experience. Hum Reprod. 1992; 7: 1067–1072. Afzelius BA, Eliasson R. Flagellar mutants in man: on the heterogeneity of the immotile-cilia syndrome. J Ultrastruct Res. 1979; 69: 43–52. Afzelius BA, Eliasson R., Johansen D., Lindholmer C. Lack of dynein arms in immotile human spermatozoa. J Cell Biol. 1975; 66: 225–232. Baccetti B., Burrini AG, Capitani S., Collodel G., Costantino-Ceccarini E., Di Cairano G., Estenoz M., Martini L., Moretti G., Piomboni P. The “short tail and stump” defect in human spermatozoa (notulae seminologicae 2). Andrologia. 1993; 25: 331–335. Baccetti B., Burrini AG, Collodel G., Magnano AR, Piomboni P., Renieri T., Sensini C. Morphogenesis of the decapitated and decaudated sperm defect in two brothers. Gamete Res. 1989; 23: 181–188. Baccetti B., Burrini AG, Collodel G., Piomboni P. Apoptosis in human ejaculated sperm cells (notulae seminologicae 9). J Submicrosc Cytol Pathol. 1996; 4: 587–596. Baccetti B., Burrini AG, Collodel G., Piomboni P., Renieri T. A “miniacrosome” sperm defect causing infertility in two brothers. J Androl. 1991; 12: 104–111. Baccetti B., Strehler E., Capitani S., Collodel G., de Santo M., Moretti E., Piomboni P., Wiedeman R., Sterzik K. The effect of follicle stimulating hormone therapy on human sperm structure (notulae seminologicae 11). Hum Reprod. 1997; 12: 1955–1968. Barthelemy C., Tharanne MJ, Lebos C., Lecomte P., Lansac J. Tail stump spermatozoa: morphogenesis of the defect. An ultrastructural study of sperm and testicular biopsy. Andrologia 1990; 22: 417–425. Bisioli C., Nodar F., Rolla ED, Papier S., Ruhlman C., Chemes HE. Peformance reproductiva mediante ICSI en hermanos no gemelos con displasia completa de la vaina fibrosa espermática. (Reproductive outcome in two brothers (not twins) with dysplasia of the fibrous sheath). In: Proceedings of the Annual Meeting of the Argentine Society of Andrology. Buenos Aires: Argentine Society of Andrology; 1999; 8 (2): 22–23. Bisson JP, Leonard C., David G. Caractere familial de certaines perturbations morphologiques des spermatozoides. Arch Anat Cytol Pathol. 1979; 27: 230–233. Blanc-Layrac G., Bringuier AF, Guillot R., Feldmann G. Morphological and biochemical analysis of cell death in human ejaculated spermatozoa. Cell Mol Biol (Noisy le Grand). 2000; 46: 187–197. Bloom E., Andersen Birch A. Ultrastructure of the “decapitated sperm defect” in Guernsey bulls. J Reprod Fertil. 1970; 23: 67–72. Olmedo Brugo S., Nodar F., Chillik C., Chemes H. Successful ICSI with sperm from a patient with dysplasia of the fibrous sheath and chronic respiratory disease. Hum Reprod. 1997; 12: 1497–1499. Olmedo Brugo S., Rawe V., Nodar F., Galaverna G., Acosta A., Chemes HE. Pregnancies established through intracytoplasmic sperm injection (ICSI) using spermatozoa with dysplasia of the fibrous sheath. Asian J Androl. 2000; 2: 125–130. Carrera A., Gerton GL, Moss SB. The major fibrous sheath polypeptide of mouse sperm: structural and functional similarities to the A-kinase anchoring proteins. Dev Biol. 1994; 165: 272–284. Chemes H. The significance of flagellar pathology in the evaluation of asthenozoospermia. In: B. Baccetti, ed. Comparative Spermatology 20 Years Later. Serono Symposia Publications, vol 75. New York: Raven Press; 1991: 815–819. Chemes H., Olmedo Brugo S., Carrere C., Oses R., Carizza C., Leisner M., Blaquier J. Ultrastructural pathology of the sperm flagellum. Association between flagellar pathology and fertility prognosis in severely asthenozoospermic men. Hum Reprod 1998; 13: 2521–2526. Chemes H., Olmedo Brugo S., Zanchetti F., Carrere C., Lavieri JC. Dysplasia of the fibrous sheath. An ultrastructural defect of human spermatozoa associated with sperm immotility and primary sterility. Fertil Steril 1987a; 48: 664–669. Chemes HE, Carizza C., Scarinci F., Brugo S., Neuspiler N., Schwarsztein L. Lack of a head in human spermatozoa from sterile patients: a syndrome associated with impaired fertilization. Fertil Steril. 1987b; 47: 310–316. Chemes H., Morero JL, Lavieri JC. Extreme asthenozoospermia and chronic respiratory disease. A new variant of the immotile cilia syndrome. Int J Androl 1990; 13: 216–222. Chemes HE, Puigdomenech ET, Carizza C., Olmedo Brugo S., Zanchetti F., Hermes R. Acephalic spermatozoa and abnormal development of the head-neck attachment. A human syndrome of genetic origin. Hum Reprod 1999; 14: 1811–1818. Escalier D., David G. Pathology of the cytoskeleton of the human sperm flagellum: axonemal and periaxonemal anomalies. Biol Cell. 1984; 50: 37–52. Evenson DP, Darzynkiewicz Z., Melamed MR. Relation of mammalian sperm heterogeneity to infertility. Science. 1980; 210: 1131–1133. Florke-Gerloff S., Topfer-Petersen E., Muller-Sterl W., Mansouri A., Schatz R., Schirren C., Schill W., Engel W. Biochemical and genetic investigation of round headed spermatozoa in infertile men including two brothers and their father. Andrologia. 1984; 16: 187–202. Gallo A., Ripoli C., Chemes HE, Coco R. Posibilidad de fertilidad en el Sindrome de Kartagener con microfertilización asistida (Fertility by ICSI in Kartagener's Syndrome). In: Proceedings of the Annual Meeting of the Argentine Society of Andrology. Buenos Aires: Argentine Society of Andrology; 1999; 8 (2): 34–35. Holstein AF, Schirren C., Schirren CG. Human spermatids and spermatozoa lacking acrosomes. J Reprod Fertil. 1973; 35: 489–491. Kjessler B. Chromosomal constitution and male reproductive failure. In: RE Mancini, L. Martini, eds. Male Fertility and Sterility. London: Academic Press; 1974: 231–247. Nistal M., Herruzo A., Corral Sanchez F. Teratozoospermia absoluta de presentacion familiar: espermatozoides microcéfalos irregulares sin acrosoma. Andrologia. 1978; 10: 234–240. Pedersen H., Rebbe H. Absence of arms in the axoneme of immotile human spermatozoa. Biol Reprod. 1975; 12: 541–544. Perotti ME, Giarola A., Gioria M. Ultrastructural study of the decapitated sperm defect in an infertile man. J Reprod Fertil. 1981; 63: 543–549. Pilder SH, Olds-Clarke P., Orth J., Jester WF, Dugan L. HSt7: a male sterility mutation perturbing sperm motility, flagellar assembly and mitochondrial sheath differentiation. J Androl. 1997; 18: 663–671. Ross A., Christie S., Edmond D. Ultrastructural tail defects in the spermatozoa from men attending a subfertility clinic. J Reprod Fertil. 1973; 32: 243–251. Sakkas D., Mariethoz E., Manicardi G., Bizzaro D., Bianchi PG, Bianchi U. Origin of DNA damage in ejaculated human spermatozoa. Rev Reprod. 1999a; 1: 31–37. Sakkas D., Mariethoz E., St John JC. Abnormal sperm parameters in humans are indicative of an abortive apoptotic mechanism linked tot he Fas-mediated pathway. Exp Cell Res. 1999b; 251: 350–355. Sakkas D., Urner F., Bizzaro D., Manicardi G., Bianchi PG, Shoukir Y., Campana A. Sperm nuclear DNA damage and altered chromatin structure: effect on fertilization and embryo development. Hum Reprod. 1998; 4: 11–19. Stalf T., Sanchez R., Kohn FM, Schalles U., Kleinstein J., Hinz V., Tielsch J., Khanaga O., Tjurley H., Gips H. Pregnancy and birth after intracytoplasmic sperm injection with spermatozoa from a patient with tail stump syndrome. Hum Reprod. 1995; 10: 21. Zamboni L. The ultrastructural pathology of the spermatozoon as a cause of infertility: the role of electron microscopy in the evaluation of semen quality. Fertil Steril. 1987; 48: 711–734. Zamboni L. Sperm structure and its relevance to infertility. Arch Pathol Lab Med. 1992; 116: 325–344. Citing Literature Volume21, Issue6November‐December 2000Pages 799-808 ReferencesRelatedInformation