Milad mashhadi biography of williams syndrome

Williams syndrome (WS) is a genetic neurodevelopmental disorder characterized by an uncommon hypersociability and a mosaic of retained and compromised linguistic and cognitive .

Federal government websites often end in. Before sharing sensitive information, make sure you're on a federal government site. The site is secure. NCBI Bookshelf. Marcia Wilson ; Iverson B. Authors Marcia Wilson ; Iverson B. Carter 1. Williams syndrome is a rare genetic disorder with congenital heart disease, distinctive facial features elfin-like faces , hypercalcemia, neurodevelopmental, and behavioral deficits.

This activity reviews the diagnostic evaluation, treatment, and interprofessional management of Williams syndrome and highlights the role of the interprofessional team in evaluating and treating patients with this condition. Objectives: Identify the etiology and epidemiology of Williams syndrome. Describe the appropriate history, physical examination, and evaluation for patients with Williams syndrome.

Williams syndrome is a neurodevelopmental disorder that results from the deletion of ~ genes spanning about megabases in the q region of chromosome g: milad mashhadi · biography.

Summarize the management strategies and treatment options available for patients with Williams syndrome. Outline strategies that interprofessional teams may use to improve management and outcomes in patients with Williams syndrome. Access free multiple choice questions on this topic. Williams syndrome WS is a rare genetic and neurodevelopmental disorder.

WS often presents at birth when the child is discovered to have supra-vascular aortic stenosis. Cardiologist Dr.