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Substantial incidence of bladder dysfunction in patients with VACTERL association: Implications for surveillance.
Gomes, Adriana; Zapata, Laura Forero; Galarreta, Carolina I; Henderson, Riley; Hoyt, Erin; Swee, Steven; Bird, Lynne M.
Afiliación
  • Gomes A; Division of Dysmorphology/Genetics, Department of Pediatrics and Rady Children's Hospital San Diego, University of California, San Diego, La Jolla, California, USA.
  • Zapata LF; Division of Dysmorphology/Genetics, Department of Pediatrics and Rady Children's Hospital San Diego, University of California, San Diego, La Jolla, California, USA.
  • Galarreta CI; Medical Genetics and Metabolism Department, Valley Children's Hospital, Madera, California, USA.
  • Henderson R; Creighton University School of Medicine, Omaha, Nebraska, USA.
  • Hoyt E; Pediatric Resident PGY-3 Valley Children's Healthcare, Madera, California, USA.
  • Swee S; Division of Extended Studies, University of California, San Diego, La Jolla, California, USA.
  • Bird LM; Division of Dysmorphology/Genetics, Department of Pediatrics and Rady Children's Hospital San Diego, University of California, San Diego, La Jolla, California, USA.
Am J Med Genet A ; 194(2): 320-327, 2024 Feb.
Article en En | MEDLINE | ID: mdl-37822287
ABSTRACT
VACTERL 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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Deformidades Congénitas de las Extremidades / Cardiopatías Congénitas / Enfermedades Renales Tipo de estudio: Incidence_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Humans Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Deformidades Congénitas de las Extremidades / Cardiopatías Congénitas / Enfermedades Renales Tipo de estudio: Incidence_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Humans Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos