Síndrome colestásico neonatal prolongado secundario a panhipopituitarismo. Informe de un caso y revisión de la literatura

摘要: Prolonged neonatal cholestasis syndrome has several etiologies, some of them are endocrinological; one these includes hypopituitarism which is infrequent and whose incidence unknown. Although isolated cases have been reported worldwide, there no reports in Mexico. We present the case a 28 day-old male who was admitted to our service with hypoglycemia. A hypophyseal hormone deficiency documented. Hormone replacement therapy started, resulted remission symptomatology. Physiopathology unclear. However, it believed that deficit growth may alter liver function decreasing biliary salt synthesis altering duct structure. The importance this stems from fact etiology should be intentionally