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Syndrome of deficiency of membrane adhesive glycoproteins
J Bartůnková1, A Fischer, A Kmínek
1Dept. of Clinical Immunology, Charles Univ. Prague, First Medical Faculty.
Abstract:
A rare autosomal recessive inherited disease is presented. Less than 100 cases were described so far (U.S.A., Europe, Japan, North Africa and Iran, respectively). The true incidence may be higher: children suffering from more serious forms of the disease may die before establishment of the diagnosis, and patients suffering from less serious forms may escape from the diagnosis. We call attention to this disease because diagnosis and therapy are available (in collaboration with institutes abroad) to patients from Czechoslovakia.