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DOI 10.1111/j.0004-8666.2002.00164.x

Медицинская библиотека · The Australian & New Zealand journal of obstetrics & gynaecology · 2002

The absence of factor V Leiden mutation in Malays with recurrent spontaneous abortions.

Yusoff Narazah Mohd, Abdullah Wan Zaidah, Ghazali Selamah, Othman Mohd Shukri, Baba Abdul Aziz, Abdullah Norazmi, Isa Mohd Nizam, Chong Chan Li

Сравнительное исследованиеСтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

OBJECTIVES

The objectives of this study were to investigate the prevalence of factor V Leiden mutation in Malay women with recurrent spontaneous abortion and to clarify the contribution of the factor V Leiden mutation to recurrent miscarriages in these women.

DESIGN

A prospective case control study between June 1999 and April 2000.

SETTING

Hospital University Science of Malaysia, Kubang Kerian, Kelantan, and Maternal and Child Health Clinic, Pasir Mas, Kelantan, Malaysia.

SAMPLES: A total of 46 Malay women with a history of three or more first or second trimester miscarriages were studied. The control group consisted of 46 parous women without obstetric complications.

METHODS

Diagnosis of factor V Leiden mutation was made by examination of factor V Leiden allele product following Mnl I digestion of factor V Leiden alleles amplified by polymerase chain reaction.

RESULTS

None of the 46 women with recurrent spontaneous abortion carried the mutation. Also, we found no subject carrying the factor V Leiden alleles in the control group.

CONCLUSION

These results suggest that that there is no association between the factor V Leiden mutation and recurrent spontaneous abortion in the Malay population.

Для цитирования: Yusoff Narazah Mohd, Abdullah Wan Zaidah, Ghazali Selamah, Othman Mohd Shukri, Baba Abdul Aziz, Abdullah Norazmi, Isa Mohd Nizam, Chong Chan Li. The absence of factor V Leiden mutation in Malays with recurrent spontaneous abortions.. The Australian & New Zealand journal of obstetrics & gynaecology. 2002. DOI: 10.1111/j.0004-8666.2002.00164.x.

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