Hernández HRJ, Rodríguez HFJ, Membrila MJ

Idioma: Español
Referencias bibliográficas: 20
Paginas: 199-201
Archivo PDF: 80.89 Kb.

RESUMEN

Se presenta un niño de tres meses con síndrome de Prader Willi (SPW). Este caso de SPW se debió a una deleción intersticial del cromosoma 15: 46, XY, del 15 (q11-q13). Reunió siete puntos de los criterios de Holm para el diagnóstico y su detección temprana permitirá un mejor pronóstico.

REFERENCIAS (EN ESTE ARTÍCULO)

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