Pregled bibliografske jedinice broj: 35232
Combined cytogenetic and Y chromosome microdeletion screening in males undergoing intracytoplasmic sperm injection
Combined cytogenetic and Y chromosome microdeletion screening in males undergoing intracytoplasmic sperm injection // Molecular human reproduction, 3 (1997), 8; 699-704 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 35232 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Combined cytogenetic and Y chromosome microdeletion screening in males undergoing intracytoplasmic sperm injection
Autori
Van der Ven, Katrin ; Montag, M. ; Peschka, B. ; Leygraaf, J. ; Schwanitz, G. ; Haidl, G. ; Krebs, D. ; van der Ven, H.
Izvornik
Molecular human reproduction (1360-9947) 3
(1997), 8;
699-704
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
ICSI; Y chromosome microdeletion
Sažetak
We evaluated the frequency of chromosomal aberrations and microdeletions of the Y chromosome in a sample of 204 patients included in an intracytoplasmic sperm injection (ICSI) programme. The prevalence of Y chromosome deletions in males with severely or only moderately reduced sparm counts is mainly unknown, so that patients were chosen with sperm counts ranging from mild oligozoospermia to azoospermia. While six out of 158 (3.8%) patients showed constitutional chromosomal aberrations, only two out of 204 (0.98%) patients were diagnosed with a microdeletion of Yq11. One had a terminal deletion in subinterval 6 of Yq11.23 which included the DAZ gene and a corresponding sperm count < 0.1 x 10(6) spermatozoa/ml. The second patient had an isolated deletion of marker Y6PH54c, a more proximal site in subinterval 5 on Yq11.23, but repeatedly showed sperm counts of 3-8 x 10(8) spermatozoa/ml. Thus, of the 158 patients who underwent a combined cytogenetic and Y-microdeletion screening, eight patients (5.1%) showed chromosomal abnormalities, either at the cytogenatic (n = 6) or the molecular level (n = 2). In conclusion, although rare in number, microdeletions of the Y chromosome can also be observed in patients with moderately reduced sperm counts. A more proximal site of the deletion breakpoint does not necessarily imply a more severe impairment of spermatogenesis than a distal deletion site. In our sample, the overall frequency of constitutional chromosomal aberrations exceeded the incidence of microdeletions of the Y chromosome even in patients with idiopathic azoo- or severe oligozoospermia.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE