Frolov Andrey, Tan Yun, Rana Mohammed Waheed-Uz-Zaman, Martin John R
Center for Anatomical Science and Education, Department of Surgery, Saint Louis University School of Medicine, 1402 S. Grand Blvd., Schwitalla Hall M-306, St. Louis, Missouri 63104, USA.
Case Rep Urol. 2018 Jun 13;2018:8293036. doi: 10.1155/2018/8293036. eCollection 2018.
Diphallia or penile duplication is a rare congenital variant with an estimated frequency of 1 per 5 to 6 million live births. The extent of duplication varies widely and typically occurs with other malformations including urogenital, gastrointestinal, and musculoskeletal anomalies. Here we present a case of human diphallia that was detected during routine dissection of an 84-year-old cadaver. Upon thorough examination, this case was characterized as a complete bifid penis which was accompanied by hypospadias with no other anatomical abnormalities detected. To gain insights into the etiology of this case, we analyzed DNA procured from the body for putative genetic variants using Next Generation Sequencing (NGS) technology. Our results support clinical observations consistent with human diphallia being a polygenic syndrome and identify new genetic variants that might underlie its etiology.
双阴茎或阴茎重复畸形是一种罕见的先天性变异,估计每500万至600万活产儿中出现1例。重复的程度差异很大,通常还伴有其他畸形,包括泌尿生殖系统、胃肠道和肌肉骨骼异常。在此,我们报告一例在对一名84岁尸体进行常规解剖时发现的双阴茎病例。经过全面检查,该病例被诊断为完全性阴茎分裂,并伴有尿道下裂,未发现其他解剖学异常。为深入了解该病例的病因,我们使用下一代测序(NGS)技术分析了从尸体获取的DNA中的假定基因变异。我们的结果支持了临床观察,即人类双阴茎是一种多基因综合征,并鉴定出可能是其病因基础的新基因变异。