U.O. di Pediatria – Ambulatorio Malattie Rare, Sindromologia e Auxologia
Dipartimento della Salute della Donna, del Bambino e dell’Adolescente
Policlinico S. Orsola-Malpighi – Area S. Orsola
Via Massarenti 9
40138 BOLOGNA
ITALIA

Lead

Pr Laura Mazzanti

Telephone: +39 051 6363723

Fax: +39 051 6363722

Mailambulatorio.malattie.rare@aosp.bo.it

Scope

Our area of expertise as ITHACA European Reference Network (ERN) centre covers all syndromes exhibiting developmental anomalies and/or intellectual disability (ID). About 1/40 newborn has a congenital malformation (261/10000 fetuses and newborn following EuroCAt reports), and 1/40 has ID. Therefore, 3 to 5 % of all human births show or will develop a developmental anomaly, among which at least 25-50% are of genetic or genomic origin. This huge population represents in reality the juxtaposition of a very large number of individually rare disorders showing an extreme diversity of causes and phenotypes. The jurisdiction and scope of expertise of this ITHACA Centre includes:

  • over 5500 dysmorphic and multiple congenital anomalie (MCA) syndromes (listed in the London Dysmorphology Database), among which over 3000 monogenic diseases, all chromosome abnormalities (most of them only detectable through array technologies), multifactorial, sporadic dysmorphological anomalies and embryofetopathies of environmental origin
  • >1500 monogenic and hundreds chromosomal forms of ID with or without associated autism spectrum disorder (ASD)

Service to patients

The regional population