Anomalía de Poland con parálisis facial periférica unilateral / The Poland anomaly with unilateral peripheral facial paralysis

The authors present the clinical history and physical findings in a 16-month baby girl with the diagnosis of Poland's syndrome associated with another congenital anomaly: unilateral peripheral facial palsy, on the opposite side. The authors believe this is the first report of such an association

Síndrome de Prader-Willi. Actualizacion diagnostica / The Prader-Willi syndrome. A diagnostic update

The authors analyze the clinical history of a 13-year-old boy with the diagnosis of Prader-Willi syndrome (PWS), who was studied in the Perinatal Pediatric Neurology and Clinical Genetics outpatient clinics, in the Social Security Arnulfo Arias Madrid Hospital Complex. The authors review the clinical characteristics that help in the diagnosis of PWS, in the neonatal period and therefore increase the rate of early diagnosis