LHX1 mutation screening in 96 patients with müllerian duct abnormalities
We sequenced LHX1 and identified a novel variation, c.1070–1081del, in 1 of 77 incomplete m€ullerian fusion patients and 1 of 105 control individuals from a Han Chinese population.
Mingdi Xia, M.Sc., Han Zhao, M.D., Ph.D., Yingying Qin, M.D., Ph.D., Yulan Mu, M.D., Ph.D., Jia Wang, M.D., Ph.D., Yuehong Bian, Ph.D., Jinlong Ma, M.D., Ph.D., Zi-Jiang Chen, M.D., Ph.D.
Volume 97, Issue 3, Pages 682-685
To investigate whether LHX1 gene mutations exist in Han Chinese patients with müllerian duct abnormalities (MDAs).
Ninety-six MDA patients and 105 control subjects from a Han Chinese population. The parents of the patients carrying the genetic variation were also screened.
Main Outcome Measure(s):
Karyotype, LHX1 gene sequencing.
We found no significant mutation in coding regions of LHX1. However, there is a new rare polymorphism of LHX1 gene, c.1070–1081del, found in 1 out of 77 incomplete müllerian fusion patients and 1 out of 105 control individuals in the Han Chinese population (thus affecting ∼1% of Han Chinese).
No causative perturbation was identified in the LHX1 gene. Mutations in the coding regions of LHX1 may not be a common genetic etiologic factor involved in Han Chinese MDA patients.
Read the full text at: http://www.fertstert.org/article/S0015-0282(11)02857-3/fulltext