DIAGNOSIS AND FOLLOW-UP OF COMPLEX CONGENITAL MALFORMATIONS/MENTAL RETARDATION (MRA/MR)
- Autori: Piro, E.; Consiglio, V.; Agrifoglio, M.; Sireci, F.; Ballacchino, A.; Salvago, P.; Martines, F.; Graziano, F.; Busè, M.; Sanfilippo, C.; Vecchio, D.; Salzano, E.
- Anno di pubblicazione: 2013
- Tipologia: Articolo in rivista (Articolo in rivista)
Complex congenital malformations, associated in 30% of cases with mental retardation, recognize different etiologies: environmental causes, mendelian disease, chromosomal abnormalities, imprinted anomalies. Frequently complex congenital disorders are rare diseases. Rare diseases are infrequent pathological conditions (prevalence in the general population of less than 1/2.000 live births1), and often poorly understood. Because of their rarity these morbid conditions often either go undiagnosed or are diagnosed late with a negative impact for both the affected person and the family. The birth prevalence is high (2-4% of all births). The diagnosis is essential to program complex and integrated care interventions (follow-up programs aimed at early detection of any disease associated with different syndromes) and to carry out proper genetic family counseling (risk of recurrence, prenatal diagnosis, detection of heterozygotes etc).