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345 Possible Causes for Fanconi Syndrome, Osteopenia and Osteoporosis

  • Osteomalacia

    CONCLUSIONS This case is of a rare association between Sjögren's syndrome, Fanconi's syndrome, and osteomalacia.[] Its causes are the same as those for Osteopenia (milder form of bone loss that usually precedes Osteoporosis.)[] WHATS IS NEW AND CONCLUSION: This case indicates that Fanconi's syndrome with osteomalacia can be acquired by a chronic hepatitis B patient taking ADV at a conventional dosage[]

  • Proximal Renal Tubular Acidosis

    It is usually associated with generalized dysfunction of the proximal tubule as part of Fanconi syndrome.[] We report a case of Fanconi syndrome and proximal renal tubular acidosis that was associated with this medication.[] Abstract To compare the difference between primary proximal renal tubular acidosis (PRTA) and Fanconi syndrome (FS), and to find out possible risk factors for growth retardation[]

  • Leukemia

    ALL, AML) Down's Syndrome Neurofibromatosis Bloom's Syndrome Klinefelter's Syndrome Fanconi's Syndrome Wiskott-Aldrich Syndrome Environmental Factors Ionizing Radiation exposure[] Bone damage – Chemotherapy or corticosteroid treatment can lead to osteopenia and osteoporosis – signs of decreased bone density, increasing the risk of fractures.[] […] and Fanconi anemia All forms of cancer that can spread within the body (malignant), including leukemia, are thought to be due to genetic abnormalities (mutations).[]

  • Renal Tubular Acidosis

    The mechanism of renal potassium wasting in renal tubular acidosis associated with the Fanconi syndrome (type 2 RTA) was investigated in 10 patients, each of whom had impaired[] Prevalence and characterization of renal tubular acidosis in patients with osteopenia and osteoporosis and in non-porotic controls.[] The prognosis for Fanconi syndrome depends on the clinical case considered.[]

  • Endocrine Dysfunction

    Final short stature, found in five of the 35 patients who attained final height, was associated with the underlying disease (specifically, Fanconi anemia) (P 0.0013), previous[] A small proportion also had osteopenia, osteoporosis, or hypercalciuria.[] A rare case report of simultaneous presentation of myopathy, Addison's disease, primary hypoparathyroidism, and Fanconi syndrome in a child diagnosed with Kearns-Sayre syndrome[]

  • Familial Hypophosphatemia

    Hereditary hypophosphatemic rickets with hypercalciuria (HHRH) and Fanconi syndrome - Unlike XLH, ADHR and ARHR, these familial disorders are considered "FGF-23 independent[] SYNDROME.[] syndrome.[]

  • Prader-Willi Syndrome

    Syndrome Syndrome, Labhart-Willi Labhart-Willi-Prader-Fanconi Syndrome Labhart Willi Prader Fanconi Syndrome Syndrome, Labhart-Willi-Prader-Fanconi Royer Syndrome Syndrome[] Fifty patients (33.8%) had osteoporosis and 41 (27.7%) had osteopenia.[] Reduced bone mineral density is typically present, and this may lead to osteoporosis and osteopenia.[]

  • Glycogen Storage Disease Type 1

    —Phosphorylase b kinase deficiency may be causally related to hepatorenal glycogenosis with the Fanconi syndrome.[] GSD1b patients on G-CSF treatment should be carefully monitored for the risk of osteopenia/osteoporosis.[] […] and sometimes osteoporosis, enlarged kidneys and platelet dysfunctions leading to frequent epistaxis (Chen, 2000; Matern et al., 2002; Rake et al., 2002).[]

  • Hypocalcemia

    Abstract We report the case of a 48-year-old man with acquired Fanconi syndrome due to IgG-kappa monoclonal gammopathy, who received a single dose of denosumab 60 mg for secondary[] When you don’t get enough calcium, you increase your risk of developing disorders like: osteoporosis osteopenia calcium deficiency disease (hypocalcemia) Children who don’[] Vitamin D resistance (rickets) - renal tubular dysfunction (Fanconi's syndrome) or receptor defect. PTH resistance - pseudohypoparathyroidism, hypomagnesaemia.[]

  • X-Linked Hypophosphatemia

    syndrome (see these terms), vitamin D deficiency and tumor-induced osteomalacia.[] […] hypophosphatemic rickets (ADHR), autosomal recessive hypophosphatemic rickets (ARHR), hereditary hypophosphatemic rickets with hypercalciuria (HHRH), fibrous dysplasia of bones, renal Fanconi[]

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