Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0013911 (emaciation)
 1,059 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The paper concerns the results of clinical trials of new specialized foods--protein, defatted and fat enpits as well as low lactose milk mixtures, which were used in dietotherapy of sick children with different disease entities (hypothrophy, bronchopulmonary abnormalities, emaciation pre- and postoperatively, mucoviscidosis, Laurence-Moon-Bardte-Biedle's syndrome, Marfan's syndrome, galactosemia, lactase deficiency). The diets including new therapeutic foods were shown to exert high therapeutic effects, that gave grounds for the methodological recommendations for using them in pediatrics to be given.
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PMID:[Clinical effectiveness of the therapeutic nutrition of sick children using enteral feeding preparations and low-lactose mixtures]. 11 35

Cystic fibrosis (CF) is the most common autosomal disorder in the Caucasian population. The main goal of the study was to assess the biological condition of adult patients with CS. Data of 90 CF patients aged 18-31 were considered. The biological condition was determined by the measurement of somatometric traits and the nutritional status. The results show a considerable physical retardation and a poor nutritional status of the studied patients. Nearly 45% of the patients showed symptoms of malnutrition, ranging from slight undernutrition to emaciation. The results, however, show a considerable variability of data among the CF patients compared with the healthy population. A significant relationship between the type of mutation and nutritional status was demonstrated.
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PMID:Biological status of adult patients with cystic fibrosis. 1921 58

The purpose of the study was to evaluate the influence of nutrition and of the severity of mutation type on survival rate in cystic fibrosis (CF) patients. Data were longitudinally collected from 60 hospitalized adult CF patients, aged 18-50. The variables consisted of body mass index (BMI) ratio, Cole's BMI cut-off points, severity of mutation type, and survival rate of CF patients. We found that the mean BMI was strongly associated with the severity of mutation type and was significantly lower in patients with severe mutations of grade I and II. The mutation type significantly affected the patients' survival rate; survival was greater in patients with mild and undefined mutation types. The BMI and Cole's cut-off points also had a significant influence on survival rate. CF patients, who suffered from malnutrition and emaciation, had a shorter survival rate than those with proper nutritional status. In conclusion, the study findings confirmed a significant effect of nutritional status and of mutation type on survival rate of CF patients.
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PMID:Survival of Patients with Cystic Fibrosis Depending on Mutation Type and Nutritional Status. 2872 79