| Update on diagnosis and monitoring of cystic fibrosis-related diabetes mellitus (CFRD). | |
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MedLine Citation:
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PMID: 22218444 Owner: NLM Status: In-Data-Review |
Abstract/OtherAbstract:
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Cystic fibrosis (CF) is the most common recessive autosomal disease among Caucasian. Children with CF have benefitted from advances in medical and nutritional treatments, and this can be gleaned from the improvement in the survival of these patients. The increase in the survival rate brought with it the appearance of co-morbidities related to CF. Nowadays cystic fibrosis-related diabetes (CFRD) is considered the most common complication associated with CF. It can appear as early as infancy or adolescence, and its prevalence can be as high as 50% in adult patients. Because of its high prevalence, difficulties in early detection and the risks involved, in recent years several studies and consensuses have focused on this condition, adding information about the epidemiology, pathophysiology, prognosis and treatment of CFRD. The main aspects of these new concepts, as well as the current recommendations for its diagnosis and follow-up, will be presented in this study. |
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Authors:
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Renata Maria de Noronha; Luís Eduardo Procópio Calliari; Neiva Damaceno; Lucia Harumi Muramatu; Osmar Monte |
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Publication Detail:
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Type: Journal Article |
Journal Detail:
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Title: Arquivos brasileiros de endocrinologia e metabologia Volume: 55 ISSN: 1677-9487 ISO Abbreviation: Arq Bras Endocrinol Metabol Publication Date: 2011 Nov |
Date Detail:
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Created Date: 2012-01-05 Completed Date: - Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 0403437 Medline TA: Arq Bras Endocrinol Metabol Country: Brazil |
Other Details:
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Languages: eng Pagination: 613-21 Citation Subset: IM |
Affiliation:
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Pediatric Endocrinology Unit, Pediatric Department, Santa Casa de São Paulo Hospital. |
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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