Since Madsen (1933) first drew attention to the possibility of serious consequences following active immunization against whooping-cough, reports of neurological sequelae of such immunization have come from various parts of the world. These sequelae (post-inoculation poliQmyelitis is not being considered here) have ranged from transient convulsions with complete recovery to gross crippling, mental retardation, and death.A survey of the literature, greatly facilitated by Kong's (1953) At 15 months grand-mal episodes became associated with the original convulsive pattern, and it was found necessary to increase the dose of phenobarbitone to 1 gr. (65 mg.) daily, and introduce phenytoin sodium, 3 gr. (50 mg.) thrice daily.Electroencephalography on May 16, 1956 (aged 19+ months), was considered diagnostic of epilepsy with the epileptic activity generalized and no focus. The main activity was in the delta range and of high frequency.At 2 years of age no significant progress had been made mentally; fits were controlled with phenobarbitone, 1 gr. (65 mg.) twice daily, and primidone, 250 mg. twice daily; and there were no focal neurological signs.At 3 years the child remained grossly retarded mentally, with no speech or understanding of speech, inability to do anything for himself, and an I.Q. of 23 on the Griffiths mental development scale. Fits were less severe and were controlled with primidone, 250 mg. twice daily, alone. Localizing neurological signs were absent, as were signs of disease elsewhere.In the accompanying review of the literature, the 107 case reports from 25 sources mentioned in Table I were examined.