SINDROME DI CORNELIA DE LANGE Aspetti genetici Gli individui con Sindrome di Cornelia de Lange (SCDL) presentano quasi sempre un corredo cromosomico completo (46 cromosomi, 23 coppie). Studi recenti indicano come modalità di trasmissione più probabile quella autosomica recessiva. Si presume una base genetica. Aspetti somatici, accrescimento fisico e sviluppo motorio sviluppo cognitivo Gli individui affetti
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