RESUMEN

OBJECTIVES: The genetic causes of pituitary stalk interruption syndrome (PSIS) remain elusive in 95 % of cases. The roundabout receptor-1 gene (ROBO1) plays critical roles in axonal guidance and cell migration. Recently, mutations in the ROBO1 gene have been reported patients with PSIS. CASE PRESENTATION: We report a 2.9-year-old boy with PSIS who presented with combined pituitary hormone deficiency, central diabetes insipidus, and the classical triad of MRI findings. Through clinical exome sequencing using next-generation sequencing techniques, a previously unidentified novel heterozygous frame shift mutation in the ROBO1 gene was identified. This is the first report of ROBO1 mutation associated with posterior pituitary dysfunction. CONCLUSIONS: We conclude and emphasize that ROBO1 should be investigated in patients with PSIS. Our case is unique in the published literature in that we are first time reporting posterior pituitary dysfunction as manifestation of ROBO1 mutation. The full clinical spectrum of the mutations may not be fully known.

Asunto(s)

Diabetes Insípida Neurogénica , Hipopituitarismo , Mutación , Proteínas del Tejido Nervioso , Receptores Inmunológicos , Proteínas Roundabout , Humanos , Masculino , Receptores Inmunológicos/genética , Receptores Inmunológicos/deficiencia , Proteínas del Tejido Nervioso/genética , Hipopituitarismo/genética , Hipopituitarismo/diagnóstico , Preescolar , Diabetes Insípida Neurogénica/genética , Hipófisis/diagnóstico por imagen , Hipófisis/patología , Hipófisis/anomalías , Pronóstico