ArticleRadiology case reports2022
Caudal regression syndrome: Postnatal radiological diagnosis with literature review of 83 cases.
Article in Radiology case reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.
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Who cites it
13 citing papers in PubMed, 15 citations in OpenAlex.
- Initially suspected case of prenatal VACTERL association ultimately diagnosed as Currarino syndrome via magnetic resonance imaging: a case description.Quantitative imaging in medicine and surgery · 2026Article
- Familial caudal regression syndrome with complex spinal dysraphism presenting as recurrent cutaneous infection.Surgical neurology international · 2026Article
- Review
- Sacral Agenesis Type II in a 12-Year-Old Patient: A Delayed Presentation in a Low-Resource Setting.Cureus · 2025Article
- Positive Evolution of a Child Suffering from Caudal Regression Syndrome and Agenesia Sacra After Treatment with Growth Hormone and Rehabilitation.International journal of molecular sciences · 2025Article
- Molecular mechanism, diagnosis, and treatment of VACTERL association.Frontiers in pediatrics · 2025Review
- Caudal regression syndrome with incidental brain tumor in a woman: A case report.Radiology case reports · 2024Article
- Radiological and clinical aspect of Caudal regression syndrome associated with dorsal hemivertebra without maternal diabetes.Radiology case reports · 2024Article
- Clinical and radiological evaluation of caudal regression syndrome.Pediatric radiology · 2024Review
- Caudal Regression Syndrome First Diagnosed in Adulthood: A Case Report and a Review of the Literature.Diagnostics (Basel, Switzerland) · 2024Article
- A 13-Year-Old Girl with Caudal Regression Syndrome and Distal Vaginal Atresia: A Case Report.The American journal of case reports · 2024Article
- Caudal Regression Syndrome-A Narrative Review: An Orthopedic Point of View.Children (Basel, Switzerland) · 2023Review
- The clinical value of prenatal ultrasound in the diagnosis of caudal regression syndrome.American journal of translational research · 2023Article
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Caudal regression syndrome (CRS) is a rare congenital disorder characterized by arrest of caudal spinal growth and associated with wide spectrum multisystemic anomalies. Herein, we presented a case of a newborn baby who did not pass meconium due to imperforated anus and was referred to the pediatric surgeon for urgent diverting loop colostomy. The conventional X-ray, abdominal ultrasound and abdominal pelvic magnetic resonance imaging (1.5 T) at 2-month-old age revealed right kidney agenesis, sacrococcygeal agenesis, vertebral bodies dysraphism and the spinal cord ends at D12-L1 with anterior and posterior bands of the terminating filaments. The diagnosis of CRS was confirmed. Through this case report, we hope to draw attention to this rare syndrome and the wide range of associated anomalies, also to consider this syndrome on the top of differential diagnosis list once the newborn has anorectal malformation mainly imperforated anus.
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