Ahmad pour mokhber biography of williams syndrome

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Ahmad pour mokhber biography of williams syndrome: Cell-based approaches, primarily mesenchymal stem

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. Summarize the management strategies and treatment options available for patients with Williams syndrome.