[Significance of LDH-determination in children with suspected myocarditis].
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Biomedical subjects
Publications and source records attributed to M Wimmer.
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It is reported about 61 children and literature of congenital heart disease and Down syndrome. Even for the cardiologist the heart malformations has to be seen only as a part of the disturbance of the whole individuum. Therapeutic problems are discussed.
Among the various types of hepatic ductular atresias, there is a group of patients with a definable syndrome of malformations: typical physiognomy, malformation of pulmonary arteries, mental retardation and disturbed growth of body and genitals. This syndrome has been defined only in the last two years by Watson et al. (1973) and Allagille et al. (1975). A detailed description of a boy with this combination of malformations is given. Additionally he has aplasia of the right kidney. A second patient out of 4, which we found in our cardiologic department, has hypoblasia of one kidney, too. The prognosis of the liver disease in these patients seems to be better than in other children with biliary atresia.
This study presents the clinical aspects as well as the therapy and prognosis of complete atrioventricular block in childhood. Our own experience is based on the case histories of 12 children with congenital complete AV block, six of them having additional heart disease and of 14 children with acquired AV block, which appeared in 10 of these children already during operation or up to 5 5/12 years after surgery.
There is given a short summary of coarctation of the aorta, with clinical picture, complications and indication for operation. Pre- and postoperative blood-pressures are correlated in the own material of 43 children.
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