METHOD AND COMPOSITIONS FOR IN VITRO DIAGNOSIS OF DISEASES DUE TO LYSOZOMIAL DEFICIENCIES, CHROMOSOMAL ABERRATIONS, MUSCULAR DYSTROPHY OR CYSTIC FIBROSIS

摘要

P PROCESS FOR IN VITRO DIAGNOSIS OF THE POTENTIALITY OR EXISTENCE OF CYSTIC FIBROSIS, MUSCULAR DYSTROPHY OR CHROMOSOMAL ABNORMALITY. IT CONSTITUTES TO CONTACT A CULTURE OF CELLS FROM THE INDIVIDUAL OR EMBRYO STUDIED WITH A COCKTAIL COMPRISING IN PARTICULAR HEPARIN, A HUMAN G-GLOBULIN, A PROSTAGLANDIN E, THEOPHYLLIN AND CYCLOHEXIMIDE, AS REGULATED PROPORTIONS IN A WAY NOT TO AFFECT SIGNIFICANTLY THE DEVELOPMENT OF CELLS, HEALTHY BUT TO CAUSE THE DEATH OF SUCH CELLS, WHEN THEY COME FROM AN INDIVIDUAL AFFECTED BY ONE OF THE ABOVE DISEASES. /P