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Updated: Aug 8, 2026

05:22
Iris Fixation via External Pentagram Suturing
Published on: May 5, 2022
Summary
This case study details diphallia, a rare congenital anomaly, alongside imperforate anus and pyloric stenosis. Such complex congenital conditions highlight the potential systemic impact of single umbilical artery findings.
Area of Science:
- Medical Genetics
- Developmental Biology
- Pediatric Surgery
Background:
- Diphallia, a rare congenital anomaly characterized by duplication of the penis, is exceptionally uncommon.
- Congenital anomalies can affect multiple organ systems, necessitating comprehensive diagnostic approaches.
- Single umbilical artery is a finding that can be associated with various other developmental abnormalities.
Observation:
- This report presents a rare case of diphallia.
- The diphallia was observed in conjunction with imperforate anus and pyloric stenosis.
- These co-occurring anomalies suggest a potential shared developmental pathway or insult.
Findings:
- The case illustrates a complex presentation of congenital malformations.
- The association of diphallia with imperforate anus and pyloric stenosis is significant.
- The findings underscore the importance of thorough evaluation in cases of single umbilical artery.
Implications:
- This case contributes to the limited literature on diphallia and its associated anomalies.
- Understanding these associations can improve diagnostic strategies for complex congenital conditions.
- Further research into the etiology of diphallia and related malformations is warranted.
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