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Complex chromosomal rearrangement involving chromosomes 1, 4 and 22 in an infertile male: case report and literature review

100%

Salahshourifar I., Shahrokhshahi N., Tavakolzadeh T., Beheshti Z., Gourabi H.

Journal of Applied Genetics

2009

tom 50

nr 1

69-72

Here we describe a rare case of an apparently balanced karyotype of 46, XY, t( 1;22;4)(p22.3;q 11.1;q31.1) in a infertile male with oligoastenoteratozoospermia (OAT). He was the second patient with complex chromosomal rearrangement (CCR) referred to our center because of infertility. We also review reports on 24 males carrying CCRs with spermatogenesis failure or a malformed child, to provide information on the reproductive outcome of male CCR carriers.

De novo complex chromosomal rearrangement of 46, XY, t[3: 16: 8] [p26: q13: q21.2] in a non-obstructive azoospermic male

72%

Salahshourifar I., Gilani M. A. S., Vosough A., Tavakolzadeh T., Tahsili M., Mansori Z., Karimi H., Totonchi M., Gourabi H.

Journal of Applied Genetics

2007

tom 48

nr 1

93-94

Complex Chromosomal Rearrangements (CCRs) are rare structural abnormalities that are usually associated with infertility or subfertility in male carriers. We described clinical and chromosomal features of a non-obstructive azoospermic male that has been referred for infertility. Cytogenetic analysis showed three chromosomes, i.e. 3, 8 and 16, which have been involved and caused spermatogenesis failure.

Ograniczanie wyników

2 Journal of Applied Genetics

2 Gourabi H.

2 Salahshourifar I.

2 Tavakolzadeh T.

1 Beheshti Z.

1 Gilani M. A. S.

1 Karimi H.

1 Mansori Z.

1 Shahrokhshahi N.

1 Tahsili M.

1 Totonchi M.

1 Vosough A.

1 2009

1 2007

Wyniki wyszukiwania

Complex chromosomal rearrangement involving chromosomes 1, 4 and 22 in an infertile male: case report and literature review

De novo complex chromosomal rearrangement of 46, XY, t[3: 16: 8] [p26: q13: q21.2] in a non-obstructive azoospermic male