[Intra-uterine dwarfism with mental retardation and malformations in the framework of alcoholic embryofetopathy. Apropos of 4 cases].
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Biomedical subjects
Publications and source records attributed to M Hermier.
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The 11th case of congenital short small intestine malrotation is described. Its clinical features associated diarrheic episodes and subobstructive symptoms. Recovery suggests that the functional adaptation of congenital and surgically-induced short small intestine may have the same quality. Neither anatomical (presence or absence of pyloric hypertrophy) nor clinical variants (obstructive and diarrheic forms) challenge the nosologic unicity of this syndrome, whose genetic character is unquestionable in most cases.
The seromucoid concentration was estimated in 131 newborn infants who were divided into four groups (controls, dysmature-postmature, infected, miscellaneous). Elevation of seromucoids suggested neonatal bacterial infection. The non-specific nature of the elevation is compensated for by the ease and the speed of obtaining a result.
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In children, nephroepithelioma represent less than 10% of the malignant tumors of the kidney. Reporting 3 cases, the authors emphasize that the clinical expression of nephroepithelioma, often made only of recurrent hematuria occuring over years, may mislead adequate diagnostic approach. Thus, a kidney arteriogram should be included in the investigations of nephroepithelioma. Earlier diagnosis may improve the rate of recovery from nephroepithelioma which, in children, is about 30%.
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