How is Prader-Willi Syndrome Diagnosed?

How is Prader-Willi Syndrome Diagnosed?

Suspicion of the diagnosis is first assessed clinically, then confirmed by specialized genetic testing on a blood sample. Formal diagnostic criteria for the clinical recognition of PWS have been published (Holm et al, 1993), as have laboratory testing guidelines for PWS (ASHG, 1996).

2017-06-20T15:48:20+00:00 June 20th, 2017|