Prevalence of vitamin K deficiency in cystic fibrosis

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چکیده

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Vitamin K in Cystic Fibrosis

The importance of vitamin K to coagulation is well known but there is increasing evidence that vitamin K has a diverse role in the body including the maintenance of bone health, preventing inappropriate calcification in soft tissues, and a protective role in inflammation. There is evidence that most, if not all, of these non-coagulation functions require higher dietary intakes than those requir...

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Vitamin D Deficiency in Cystic Fibrosis

Cystic Fibrosis is the most common inherited genetic respiratory disorder in the Western World. Hypovitaminosis D is almost universal in CF patients, likely due to a combination of inadequate absorption, impaired metabolism, and lack of sun exposure. Inadequate levels are associated with the high prevalence of bone disease or osteoporosis in CF patients, which is associated with increased morbi...

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Vitamin K supplementation for cystic fibrosis.

BACKGROUND Cystic fibrosis is a genetic disorder which can lead to multiorgan dysfunction. Malabsorption of fat and fat-soluble vitamins (A, D, E, K) may occur and can cause subclinical deficiencies of some of these vitamins. Vitamin K is known to play an important role in both blood coagulation and bone formation. Supplementation with vitamin K appears to be one way of addressing the deficienc...

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Prevalence of Cystic Fibrosis Trans-membrane Conductance Regulator Gene common mutations in children with cystic fibrosis in Isfahan, Iran

Background: Cystic fibrosis (CF) is the most common lethal genetic disorder of Cystic Fibrosis Trans-membrane Conductance (CFTR) Regulator gene mutations. We aimed to investigate common mutations in CF patients and to assess its possible relationship with clinical presentations. Materials and Methods: This cross sectional study was conducted on 36 CF patients who were referred to a tertiary ped...

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Iron deficiency in cystic fibrosis.

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ژورنال

عنوان ژورنال: The American Journal of Clinical Nutrition

سال: 1999

ISSN: 0002-9165,1938-3207

DOI: 10.1093/ajcn/70.3.378