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Compound heterozygous mutations in PMFBP1 cause acephalic spermatozoa syndrome:A case report
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作者 Tian-Qin Deng yu-li xie +2 位作者 Jiang-Bo Pu Jiang Xuan Xue-Mei Li 《World Journal of Clinical Cases》 SCIE 2022年第34期12761-12767,共7页
BACKGROUND Acephalic spermatozoa syndrome(ASS)is an extremely rare form of severe teratozoospermia,where in most of the sperm either appear to lack heads or have disconnected or poorly connected heads and tails.CASE S... BACKGROUND Acephalic spermatozoa syndrome(ASS)is an extremely rare form of severe teratozoospermia,where in most of the sperm either appear to lack heads or have disconnected or poorly connected heads and tails.CASE SUMMARY We reported the case of a male patient with secondary infertility whose sperm showed typical ASS upon morphological analysis.Whole-exome sequencing was performed on the patient’s peripheral blood,which revealed two heterozygous variants of the PMFBP1 gene:PMFBP1c.414+1G>T(p.?)and PMFBP1c.393del(p.C132Afs*3).CONCLUSION It is speculated that the compound homozygous mutation of PMFBP1 may be the cause of ASS.We conducted a literature review in order to provide the basis for genetic counseling and clinical diagnosis of patients with ASS. 展开更多
关键词 Acephalic spermatozoa syndrome PMFBPI INFERTILITY Male SPERM Case report
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