Lageron A, Mazière J C, Gane P, Goossens D, Roy C
INSERM Paris.
Acta Histochem. 1992;92(1):39-45. doi: 10.1016/s0065-1281(11)80139-x.
A case of storage disease followed up during 12 a was studied by morphological, histochemical, immunological, and biochemical techniques. Data were analysed in an attempt to differentiate an acquired storage by excessive cell degradation from a storage of genetic origin. If, as it is our belief, a conclusion of acquired storage can be made, this observation in which the same cholesterol metabolism abnormalities as in Niemann Pick type C were seen, leads to a rediscussion of their diagnostic significance.