21 marzo 1881 anni - Tay sachs disease
Descrizione:
hereditary neurodegenerative disorder resulting from excess storage of GM2 ganglioside within the lysosomes of cellsgenetic mutation known as the HEXA mutation results in the body not producing an enzyme called Hexosaminidase-A (Hex-A).
Aggiunto al nastro di tempo:
Data:
21 marzo 1881 anni
Adesso
~ 144 years ago