A familial case of VACTERL association with co-occurring sacrococcygeal teratoma: a case report
Skillful personnel and equipment to detect the anomalies in-utero and the use of modern DNA sequencing techniques to detect the possible underlying genetic defects can help us better understand the pathophysiology of various congenital disorders. Early diagnosis is crucial for optimizing management strategies and counselling parents regarding potential outcomes.
Authors
- Razia Iftikhar
- Khabab Abbasher Hussien Mohamed Ahmed (ORCID: https://orcid.org/0000-0003-4608-5321)
- Erum Ilyas (ORCID: https://orcid.org/0009-0003-6095-9782)
- Muhammad Affan (ORCID: https://orcid.org/0009-0007-9841-7830)
Institutions
- University of Khartoum (SD)
- Jinnah Sindh Medical University (PK)
- Sir Syed University of Engineering and Technology (PK)
Publication Details
- Journal
- Oxford Medical Case Reports
- Published
- 2025-05-01
- DOI
- https://doi.org/10.1093/omcr/omaf046
- Primary Topic
- Esophageal and GI Pathology
- Type
- article
- Field-Weighted Citation Impact
- 0.00