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Síndrome de Pallister-Killian en una paciente mestiza mexicana: Reporte de caso

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0 Published in 2018 at "Archivos Argentinos De Pediatria"

DOI: 10.5546/aap.2018.e135

Abstract: Pallister-Killian syndrome is caused by a tetrasomy 12p mosaicism and is characterized by facial dysmorphism, pigmentary skin anomalies, congenital heart defects, diaphragmatic hernia, epilepsy and mental retardation. The diagnosis is complex as the cytogenetic analysis… read more here.

Keywords: pallister; paciente mestiza; pallister killian; ndrome pallister ... See more keywords