Substantial incidence of bladder dysfunction in patients with VACTERL association: Implications for surveillance

Author:

Gomes Adriana1ORCID,Zapata Laura Forero1,Galarreta Carolina I.2ORCID,Henderson Riley3,Hoyt Erin4,Swee Steven5,Bird Lynne M.1ORCID

Affiliation:

1. Division of Dysmorphology/Genetics, Department of Pediatrics and Rady Children's Hospital San Diego University of California, San Diego La Jolla California USA

2. Medical Genetics and Metabolism Department Valley Children's Hospital Madera California USA

3. Creighton University School of Medicine Omaha Nebraska USA

4. Pediatric Resident PGY‐3 Valley Children's Healthcare Madera California USA

5. Division of Extended Studies University of California, San Diego La Jolla California USA

Abstract

AbstractVACTERL association is defined as the nonrandom co‐occurrence of a minimum of three of the following six key components: Vertebral anomalies, Anal atresia, Cardiac malformations, Tracheo‐Esophageal fistula, Renal anomalies, and Limb abnormalities. Patients presenting with two components may also belong in the same spectrum. Additional components have been associated with VACTERL defects, including single umbilical artery, tethered spinal cord (TSC), and genital malformations. We observed a significant proportion of patients with bladder dysfunction (often called neurogenic bladder in the medical record) when reviewing a cohort of patients with VACTERL defects at our clinical center. Our finding calls attention to bladder dysfunction as an additional VACTERL phenotypic component. The prevalence of bladder dysfunction is greatest in those with genital anomalies, anorectal malformations, sacral dysplasia, renal anomalies, and TSC. We propose that patients with two or more VACTERL malformations be monitored for symptoms of bladder dysfunction if one or more of the identified risk factors are present until the achievement of urinary continence.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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