ABSTRACT
Trisomy 11q in a 13-month-old patient with severe mental deficiency, generalized dysmorphia, and a cardiac anomaly represents a previously unrecognized form of malsegregation of the frequently observed translocation t(11;22)(q23.1;q11.1).
Subject(s)
Chromosome Aberrations , Translocation, Genetic , Trisomy , Chromosomes, Human, 21-22 and Y , Chromosomes, Human, 6-12 and X , Humans , Infant , Intellectual Disability/genetics , MaleABSTRACT
The isoenzyme content of creatine kinase was determined in various human organs after autopsy. The results found were on the whole in agreement with the literature. Their analysis dictates the choice of a method of separation of the MB fraction: chromatography or electrophoresis. It permits better interpretation of the results of estimation of the MB fraction in the serum.
Subject(s)
Creatine Kinase/analysis , Brain/enzymology , Chromatography , Creatine Kinase/blood , Digestive System/enzymology , Electrophoresis , Female , Humans , Isoenzymes , Lung/enzymology , Male , Muscles/enzymology , Myocardium/enzymology , Pancreas/enzymology , Prostate/enzymology , Thyroid Gland/enzymology , Uterus/enzymologyABSTRACT
A case of renal metastases from epidermoid bronchial cancer, discovered during an attack of hematuria, is reported. The patient had been operated upon for bronchial cancer two years ago and was in good general condition. Au I.V.U. showed the presence of an ill-defined renal mass. Selective renal arteriography demonstrated that the mass was hypervascularized and that a previous injection of angiotensin produced a malignant type of hypervascularization in the mass.
