Синдром на Прадер-Вили [Health Category:
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“Синдромът на Прадер-Вили е сравнително рядко генетично заболяване, при което седем гена в сегмент 15q11 – 13 на 15-а хромозома вкупом или частично са делетирани или не се експресират. За пръв път е описан през 1956 г. от швейцарските лекари:Андреа Прадер, детски ендокринолог
Хайнрих Вили, педиатър
Гуидо Фанкони, педиатър
Алексис Лабхарт (1916), невролог и
Андрю Циглер, патолог. …” (Wikipedia) (Wikipedia translated)
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