Williams-Beurin syndrome added to Atlas of Human Malformation Syndromes in Diverse Populations

NHGRI researchers and their international collaborators have added Williams-Beuren syndrome to theAtlas of Human Malformation Syndromes in Diverse Populations. By adding highly accurate images and clinical information of diverse people with Williams-Beuren Syndrome, healthcare providers will better recognize and diagnose the rare disease in non-Europeans and deliver critical, early interventions and better medical care. Results are published in the May 2018 issue of theAmerican Journal of Medical Genetics.

Source: NHGRI Homepage Highlights - May 2, 2018 Category: Genetics & Stem Cells Source Type: news