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

نویسندگان

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

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).

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عنوان ژورنال:

دوره 11  شماره 

صفحات  -

تاریخ انتشار 2013