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Медицинская библиотека · Iranian journal of reproductive medicine · 2013

Identification of Xq22.1-23 as a region linked with hereditary recurrent spontaneous abortion in a family.

Shekouhi Sahar, Baghbani Fatemeh, Hasanzadeh Nazar-Abadi Mohammad, Hamzehloie Tayebeh, Abbaszadegan Mohammad Reza, Saghafi Nafiseh, Raoofian Reza, Zavar Reza Javad, Ahmadzadeh Shahab, Tabatabaiefar Mohammad Amin, Mojarrad Majid

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Аннотация

BACKGROUND

Recurrent spontaneous abortion (RSA) is one of the most common health complications with a strong genetic component. Several genetic disorders were identified as etiological factors of hereditary X linked RSA. However, more genetic factors remain to be identified.

OBJECTIVE

In this study we performed linkage analysis on a large X linked RSA pedigree to find a novel susceptibility locus for RSA.

MATERIALS AND

METHODS

A linkage scan using 11 microsatellites was performed in 27 members of a large pedigree of hereditary X-linked RSA. Two point parametric Linkage was performed using Superlink v 1.6 program.

RESULTS

Evidence of linkage was observed to markers at Xq23, DXS7133 and at Xq22.1 DXS101, with LOD score of 3.12 and 1.60, respectively.

CONCLUSION

Identified locus in this study may carry a responsible gene in RSA. Narrowing down of this region may leads to identification of this gene. This article extracted from M.Sc. thesis. (Sahar Shekouhi).

Для цитирования: Shekouhi Sahar, Baghbani Fatemeh, Hasanzadeh Nazar-Abadi Mohammad, Hamzehloie Tayebeh, Abbaszadegan Mohammad Reza, Saghafi Nafiseh, Raoofian Reza, Zavar Reza Javad, Ahmadzadeh Shahab, Tabatabaiefar Mohammad Amin, Mojarrad Majid. Identification of Xq22.1-23 as a region linked with hereditary recurrent spontaneous abortion in a family.. Iranian journal of reproductive medicine. 2013.
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