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Iranian journal of reproductive medicine · 2013

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

СтатьяНазвание и аннотация: Перевод в очереди
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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

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).

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

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