## Abstract Williams syndrome (WS) is a genetic neurodevelopmental disorder, most often accompanied by mildβtoβmoderate mental retardation. Individuals with WS show unique communication strengths and impairments that are challenging to treat in community, educational, and vocational settings. Many
Otitis media with effusion and hearing loss in children with Cornelia de Lange syndrome
β Scribed by Paola Marchisio; Angelo Selicorni; Lorenzo Pignataro; Donatella Milani; Elena Baggi; Lara Lambertini; Elisa Dusi; Laura Villa; Pasquale Capaccio; Marta Cerutti; Susanna Esposito; Nicola Principi
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 98 KB
- Volume
- 146A
- Category
- Article
- ISSN
- 1552-4825
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π SIMILAR VOLUMES
## Abstract Hearing loss is common in schoolβage individuals with Williams syndrome (WS) and extensive in adults. Prior studies with relatively small sample sizes suggest that hearing loss in WS has an early onset and may be progressive, yet the auditory phenotype and the scope of the hearing loss
## Abstract Cornelia de Lange syndrome (CdLS) is a multisystem congenital anomaly disorder characterized by prenatal and postnatal growth retardation, developmental delay, distinctive facial dysmorphism, limb malformations, and multiple organ defects. Mutations in the __NIPBL__ gene have been disco