Syphilis and Congenital Mental Defect

1911 ◽  
Vol 57 (238) ◽  
pp. 499-506 ◽  
Author(s):  
C. G. A. Chislett

With the exception of cretinism, mongolism and amaurotic idiocy, and juvenile general paralysis, it may be said that the only classification of congenital mental deficiency is one based on the degree of mental defect.

1951 ◽  
Vol 97 (408) ◽  
pp. 468-479
Author(s):  
E. O. Lewis

Mental deficiency and its synonym “oligophrenia” are terms interpreted very differently in various countries; this has made it almost impossible to compare the statistical data of these countries. The concept the lay person in this country has of mental defect applies with few exceptions to individuals with intelligence quotients below 60 per cent., i.e., idiots, imbecile and obvious simpletons. When a person with this conception of mental defect—and we must admit that it corresponds fairly closely to the legal interpretation of the Mental Deficiency Acts in this country—is told that mental deficiency is a major social problem, the statement is received with some measure of incredulity. There is some justification for this incredulity. The statement is ambiguous and is based upon some rather muddled thinking. If we accept this legal and administrative interpretation of mental defect only about 1 per cent. of the population can be said to be mentally defective. Probably no other 1 per cent. of the population has such a high proportion of decent, docile and law-abiding citizens. If so, what meaning can we give to the statement that mental deficiency is a major social problem ?


PEDIATRICS ◽  
1952 ◽  
Vol 9 (2) ◽  
pp. 204-211
Author(s):  
HERMAN YANNET ◽  
FRANK HORTON

The relative importance of the hypotonic type of cerebral palsy among the mentally defective is stressed. This type of cerebral palsy manifests itself in either of three clinical pictures with some overlapping, namely, atonic, ataxic and athetoid. The etiology is variable in each of these groups and may be effective in either the prenatal, paranatal or postnatal periods. The severity of the mental defect, the high incidence of convulsive disorders, and the tendency toward microcephaly point towards the widespread nature of the pathologic process regardless of etiology. The syndrome of atonic diplegia, as herein described, is probably invariably associated with the more severe degrees of mental deficiency.


1915 ◽  
Vol 22 (4) ◽  
pp. 492-516 ◽  
Author(s):  
Henry A. Cotton

From the data provided by our investigations we may conclude that in all pathologic processes of the cortex which end in dementia and death, the fatty degeneration of the elements of the cortex plays a not unimportant part. The characteristic change for most of the psychoses is found in a great increase in amount of fatty deposits when compared to normal individuals of the same age. In some processes such as senile dementia and dementia præcox the fatty substance appears to fill completely the cell body, and these cells have apparently lost all their functioning power. It is not common to find the fatty deposits in the processes of the ganglion cells except in dementia præcox, and to a limited extent in senile dementia. In other cases the pathological variety of the fatty deposits in the ganglion cells is seen to be diffused over the whole ganglion cell. We were able especially to observe this in infectious psychoses, in general paralysis, and in epilepsy. The so called central neuritis assumes a peculiar attitude in that it plainly leads swiftly to an acute fatty degeneration of the ganglion cells, in which there exists an inclination of the fatty granules to flow together into large masses. Frequently the fatty degeneration of the ganglion cells appears to be connected with the sclerosis of the cells, especially when it is a matter of slowly progressing alterations of degeneration. The behavior of the glia is not wholly uniform in the various disease processes. In chronic disease processes we often find that the extent of the fatty accumulations in the ganglion cells does not correspond to an equal increase in the glia cells, while the otherwise acutely degenerative alteration in the nuclei of the glia is noticeable. In acute processes we see regularly an equal accumulation of the fat in both species of cell. The conditions of the cells in the vascular wall are wholly similar to those of the glia cells. We must therefore assume that in chronic diseases the fatty substance has been carried out of the glia and the vascular walls while it has been retained longer in the ganglion cells. Among all the disease processes amaurotic idiocy assumes a peculiar position. We have observed that in addition to the fatty materials of the scarlet fat stain, still other fatty materials, lipoid in character, have made their appearance. While the study of the fatty deposit in the cerebral cortex offers some points for a differential diagnosis, yet it is not adopted in all cases, since the distinction in individual disease processes is not always characteristic. From the preceding examination, however, in many cases there result important findings which briefly we summarize as follows: 1. In all degenerative alterations in the cerebral cortex the mass of the lipoid materials in the ganglion cells in comparison with that in healthy individuals of equal age is found to be considerably augmented. In the alteration of the lipoid materials in the ganglion cells two types in general may be distinguished: (a) An augmentation of the lipoid materials in the ganglion cells, in places where normally a small amount of fat is found, (b) An augmentation of the lipoid materials over the entire cell. 2. The first type we find also characteristic in senile dementia. The second type occurs in acute infectious psychoses, general paralysis, and well advanced epilepsy. 3. While the advanced lipoid degeneration of the ganglion cells in senile dementia has already been described in many ways, it has appeared from our investigations that also in the young chronic cases of dementia præcox far-reaching fatty degeneration of the ganglion cells, especially in the second and third cortical strata, likewise occurs. These findings should constitute an important contribution to the pathological anatomy of dementia præcox. 4. The so called central neuritis represents a peculiar disease process according to the appearance of the fatty degeneration, since this fatty degeneration reaches a very advanced degree, and also in so far as it deviates from other disease processes in that here there comes out very distinctly in the picture an inclination of the fatty granules to flow together. 5. Amaurotic idiocy also represents a particular disease process in respect to the lipoid degeneration, since here in addition to otherwise distributed scarlet stain lipoid materials, still other specific lipoid materials make their appearance.


1958 ◽  
Vol 104 (434) ◽  
pp. 91-102 ◽  
Author(s):  
A. H. Tingey ◽  
R. M. Norman ◽  
H. Urich ◽  
W. H. Beasley

The customary classification of the amaurotic family idiocies according to the time of life at which neurological signs first appear has obvious limitations when consideration is given to cases occupying an intermediate position between the well-established infantile form of Tay-Sachs' and the juvenile form first described by Batten (1903). It was to this group of atypical cases that Bielschowsky (1913–14, 1920) gave the name “late infantile”. This term is convenient clinically but when more examples of the variant had been reported it became evident that the group of cases so designated was not homogeneous. Wyburn-Mason (1943) was able to show in a large clinical material that many of these intermediate forms belonged either to families affected by Tay-Sachs' or by Batten's disease and that in an individual case the ophthalmological findings were usually of decisive importance in classification. The existence of a precocious variant of the classical “juvenile” type of amaurotic idiocy was thus clearly established. Klenk's (1939) discovery that the nerve cells in Tay-Sachs' disease contain large amounts of a glycolipid subsequently called “ganglioside” has provided a further valuable criterion in distinguishing this form of lipidosis from other members of the group. The present case, an example of the precocious juvenile type of amaurotic idiocy or, as we prefer to name it, the subacute form of Batten's disease, is presented as a further contribution to this subject.


1963 ◽  
Vol 9 (5) ◽  
pp. 566-572 ◽  
Author(s):  
J L Karlsson

Abstract A new approach is described for the detection of abnormal metabolites in the urine of patients with known or suspected metabolic disorders. Distribution curves are presented for nonurea organic carbon and nitrogen which form a basis for judging whether grossly abnormal amounts of organic materials are present in the urine. Families with recurrent mental retardation have been identified whose mental defect may be on an unknown metabolic basis.


1921 ◽  
Vol 67 (279) ◽  
pp. 475-482
Author(s):  
G. A. Auden

When our President invited me to contribute a paper for this meeting, I understood that it was to be of the nature of a presentation of the case of the school medical officer in relation to a unification of those medical services which deal with the various aspects of mental defect. This I have attempted to do in the belief that if real constructive work is to be done, the foundations must be laid by examining the problem as it is manifested in childhood and early youth. This is comparatively easy, because not only does a very large proportion of children and young persons now come under continuous medical observation, but there is in addition the important testimony which their educational progress affords as to their mental make-up. Further, I believe that the practical solution of the question of mental deficiency from the point of view of the community at large will depend for its completeness upon early diagnosis, and upon the measures which are taken to deal with the subjects before they reach adult life. In one of his addresses, Dr. Oliver Wendell Holmes urges that in these days of specialisation we must not neglect the older theories which have yielded place to new. “The débris of broken systems and exploded dogmas form a great mound, a Monte Testaccio of shards and remnants of old vessels which once held human beliefs. If you take the trouble to climb to the top of it, you will widen your horizon.” To none is this advice more needful than to those of us who are brought into contact with mental defect and all its attendant problems. There is still so much confusion of thought, the result of changing points of view, that we do not always see clearly the end to which our efforts should be directed. This is of practical importance, because upon the standpoint from which we view the problem will depend, not only the range of our activities, but also the particular members of the community whom we hope to include therein.


1939 ◽  
Vol 85 (359) ◽  
pp. 1183-1193 ◽  
Author(s):  
Max Hayman

The development of the concepts underlying the terms mental deficiency and psychosis with mental deficiency, may be arbitrarily divided into four periods, which to a considerable degree, overlap. The first period is concerned with the separation of the two principal groups, mental deficiency and mental disorder. Even before the time of Hippocrates some differentiation had been made between the idiot, who was feeble-minded from birth and the dement, who had deteriorated from a previously normal status. Pinel (1), however, as late as 1806 used the term idiocy loosely, and included many cases of terminal dementia and other deteriorated states. The end of the first period is marked by the definitive separation by Esquirol (2), in 1828, of mental defect and mental disorder, but it was not till 1886, in England, that a legal differentiation was made been insanity and feeble-mindedness.


1970 ◽  
Vol 116 (533) ◽  
pp. 369-375 ◽  
Author(s):  
L. S. Penrose

The study of mental deficiency can be said to be based upon measurement. It is biometrical in a way that the rest of psychiatry is not, because the ultimate criteria for diagnosis of mental defect (or subnormality) are quantitative. Some kind of intelligence measurement or rating is always implied, and even at the lowest level quite often a measurement is actually made. In this lecture I shall only be able to outline my subject by giving examples.


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