| dc.contributor | Salinas-Torres, V.M., Servicio de Genética Médica, Hospital Civil Fray Antonio Alcalde, Guadalajara, Jalisco, Mexico, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Mexico; Ramos-Márquez, C.M.E., Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Mexico; Serra-Ruiz, L., Servicio de Neonatología, Hospital Civil Fray Antonio Alcalde, Guadalajara, Jalisco, Mexico; Angulo-Castellanos, E., Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Mexico, Servicio de Neonatología, Hospital Civil Fray Antonio Alcalde, Guadalajara, Jalisco, Mexico | |
| dc.description.abstract | VACTERL-H syndrome is a complex disorder of congenital malformations that implies vertebrae, anus, heart, trachea, esophagus, kidneys, limbs and hydrocephalus. Its etiology has been identified in a fraction of patients largely due to their sporadic nature and its high degree of clinical heterogeneity. This report presents a newborn with VACTERL-H syndrome, associated with unusual branchial arch, dermoepidermal and nervous system anomalies, which are compared with those described in the medical literature. Based on our experience, the presentation of this case not only expands the knowledge of the spectrum of anomalies that can occur in VACTERL-H syndrome, but also can be useful in identifying patients with this heterogeneous phenotype. | |
