The Arid Melancholy- Netherton Syndrome With Protein Energy Malnutrition
نویسندگان
چکیده
منابع مشابه
[Netherton syndrome].
The authors reported a case of Netherton's syndrome. This patient presented cutaneous lesions of ichthyosis linearis circumflexa, tricorrexis invaginata and atopy signs associated with cystinuria. Cutaneous and hair lesions were treated with etretinate.
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Objective: The aim of this study was to find out the prevalence of protein energy malnutrition(PEM) by anthropometric measurements in preschool children of tribal community of Chhattisgarh. Material and Methods: A total of 449 children [237 boys and 212 girls] from 286 families were selected randomly. Anthropometric measurements were done as per standard protocol. The level of underweight, stun...
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The use of a high-fat diet in malnourished children produced accelerated growth of lean tissues as well as adipose tissue, and resulted in rapid nutirtional rehabilitation in 25 seriously malnourished babies. Such diets are easy to prepare and relatively cheap, and they offer important advantages over conventional feeding in the hospital treatment of malnourished children.
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Netherton syndrome is a rare autosomal recessive condition with variable expression. It comprises an ichthyosiform dermatitis and erythroderma of variable intensity associated with hair abnormalities and features of atopy. The pathognomic (required for diagnosis) feature is trichorrhexis invaginata identified by microscopic examination of hair shaft. Ichthyosis linearis circumflexa is ano...
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I . The ‘big’ insulin content of the serums from ten children with protein-energy malnutrition was estimated before, during and after 3-6 weeks of treatment. The valucs for immunoreactive insulin (IRI) after intravenous injections of glucose were almost normal, with one exception, although tolerance was impaired. In addition, total body potassium content (TBK) was measured for three of the chil...
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ژورنال
عنوان ژورنال: JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH
سال: 2016
ISSN: 2249-782X
DOI: 10.7860/jcdr/2016/18200.7655