口腔黏膜测试
生物
核型
X染色体
遗传学
基因型
男科
精液分析
染色体
不育
怀孕
基因
医学
作者
Mahshad Magharehabed,Navid Almadani,Masomeh Askari,Masoumeh Naji,Arvand Akbari,Hamid Gourabi,Mohammad Ali Sadighi Gilani,Fakhredin Reyhani Sabet,Najmehsadat Masoudi,Mehdi Totonchi
出处
期刊:Andrologia
[Wiley]
日期:2019-04-17
卷期号:51 (7): e13290-e13290
被引量:7
摘要
Chimerism, a rare human disorder, is assumed to be the result of an amalgamation of two separate zygotes in a single embryo. Studies have shown that the phenotypic spectrum of chimerism is variable and there is no definite genotype-phenotype correlation in patients with chimerism, therefore a majority of cases might remain undiagnosed. This study aims to investigate the possible mechanism of the chimerism in a 46,XX/46,XY infertile and phenotypically normal male, with 46,XX blood karyotype and normal spermatogenesis. We have used Interphase-FISH analysis to study the CEPX and CEPY regions on buccal and urine samples as well as molecular analysis of polymorphic short tandem repeats (STR) markers from 34 loci in order to discover the origin of 46,XX/46,XY. Analysis of X-linked and autosomal STR markers on blood, buccal tissue, urine, fibroblast and testis biopsy samples of the proband along with the blood sample of the patient's parents and siblings, showed divergent karyotypes in different tissues and tetragametic chimerism was diagnosed.
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