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Chromosome 12;15 rearrangements in patients with recurrent miscarriage.
Indian J Hum Genet ; 2006 Sept; 12(3): 133-139
Article in English | IMSEAR | ID: sea-143314
ABSTRACT

Background:

An abnormal karyotype in either partner, especially featuring a translocation and/or inversion is considered to be a cause of recurrent miscarriages. It is generally assumed that recurrent miscarriage might be due to recurrent chromosomal abnormalities in the fetus due to a balanced aberration in one of the parents being inherited by the offspring in an unbalanced form.

Aim:

Evaluation of chromosomal rearrangements in couples with recurrent miscarriages. Materials and

Methods:

Peripheral blood was collected and lymphocyte cultures were set up. Slides prepared from the cell suspension were stained and screened for metaphases followed by karyotyping.

Result:

Balanced translocation was observed in the male partner in one case and in the female partners in the three other cases.

Conclusion:

Couples with recurrent miscarriage should be investigated for chromosomal rearrangements, thus helping in genetic counseling and providing the options for future pregnancies.

Full text: Available Index: IMSEAR (South-East Asia) Language: English Journal: Indian J Hum Genet Year: 2006 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Language: English Journal: Indian J Hum Genet Year: 2006 Type: Article