Treatment of Familial Hypophosphatemia
نویسندگان
چکیده
منابع مشابه
Familial Hypercholesterolemia: From Diagnosis to Treatment
Familial hypercholesterolemia (FH) is an inherited common autosomal Mendelian disorder of lipoprotein metabolism with a population prevalence of 1 in 500. FH is characterized by severely elevated levels of low-density lipoprotein cholesterol (LDL-C), which result in surplus deposition of cholesterol in tissues. This condition leads to premature at hero sclerosis and early-onset of coronary hear...
متن کاملTreatment of hypophosphatemia in the intensive care unit: a review
INTRODUCTION Currently no evidence-based guideline exists for the approach to hypophosphatemia in critically ill patients. METHODS We performed a narrative review of the medical literature to identify the incidence, symptoms, and treatment of hypophosphatemia in critically ill patients. Specifically, we searched for answers to the questions whether correction of hypophosphatemia is associated...
متن کاملMetabolism of vitamin D3-3H in vitamin D-resistant rickets and familial hypophosphatemia.
The fate of an intravenous dose of tritiated vitamin D(3) was studied in seven normal subjects, four children with vitamin D-resistant rickets, and four adults with a familial history of vitamin D-resistant rickets and persistent hypophosphatemia. An abnormal metabolism of vitamin D in vitamin D-resistant rickets was defined and characterized by a decrease in the plasma fractional turnover rate...
متن کاملRespiratory illness and hypophosphatemia.
We retrospectively reviewed the charts of 308 admissions to a pulmonary disease ward and 100 admissions to the general medical service over one year to find the prevalence, sequelae, and etiology of hypophosphatemia. The overall prevalence of low serum phosphate levels (less than 2.4 mg/dl) occurring at least once during hospitalization in chest patients was 17 percent, but was higher in patien...
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ژورنال
عنوان ژورنال: Orthopedics & Traumatology
سال: 1980
ISSN: 1349-4333,0037-1033
DOI: 10.5035/nishiseisai.28.639