Descriptor Portuguese: Hipofosfatemia Familiar. Synonyms English: Diabetes, Phosphate Familial Hypophosphatemia Hyperphosphaturia Phosphate Diabetes. [] Hipofosfatemia familiar Nefrocalcinose Nefrolitíase Osteomalácia Raquitismo Raquitismo hipofosfatêmico familiar Tomografia. Meanings of “hipofosfatemia” in English Spanish Dictionary: 1 result(s) Medicine. 1, Medicine, hipofosfatemia familiar · familial hypophosphatemia.

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HLA-antigens in a Tunisian familial chondrocalcinosis.

hipofosfatemia familiar pdf

Mutations in ANKH cause chondrocalcinosis. Hum Mol Genet 4: J Pathol ; Transforming factor b stimulation of parathyroid hormone-related protein PTHrP: Mol Cell Endocrinol ;; Hereditary pyrophosphate arthropathy familial articular chondrocalcinosis in Sweden. A thymoma as a cause of true ectopic hyperparathyroidism. Hereditary articular chondrocalcinosis in the Osona region Barcelona: Adams JS, Diz MM, Sharma OP, Effective reduction in the serum 1,dihydroxyvitamin D and calcium concentration in sarcoidosis-associated hypercalcemia with short-course chloroquine therapy.

A newly famkliar syndrome. All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. Tumor necrosis factor enhances parathyroid hormone-related protein PTHrP -induced hypercalcemia and bone resorption without inhibiting bone formation in vivo.

Calcitriol production in hypercalcemic and normocalcemic patients with non-Hodgkin lynfoma.

Eur J Cancer ; Familial articular chondrocalcinosis is a disorder characterized by deposition of calcium pyrophosphate dihydrate crystal in synovial fluid and articular cartilage that can cause joint pain and arthritis. Eur J Haematol ; Familial chondrocalcinosis seems to be rare in Brazil, but we do not exclude the possibility that this figure is underestimated and suggest that in cases of sporadic chondrocalcinosis other members of the family should be fully investigated.


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An example of resorp-tive hypercalciuria. Hereditary hyperparathyroidism-jaw tumor syndrome: Hypercalcemia and elevated 1,dihydroxyvitamin D levels in a patient with end-stage renal disease and actve tuberculosis.

Hyperthyroidism with coexisting hyperparathyroidism.

Av Brigadeiro Luiz Antonio, – Cj Curr Opin Rheumatol Ann Intern Med ; Hypercalcemia is a common underdiagnosed metabolic abnormality, since it is frequently asymptomatic. Idiopathic familial chondrocalcinosis due to apatite crystal deposition. Hipofosfatema D conversion by sarcoid lymph node homogenate. Stimulation by parathyroid hormone-related protein and transforming growth factor a of phosphate transport in osteoblast-like cells.

The effect of short-term lithium administration of supressibility of parathyroid hormone secretion by calcium in vivo. Ectopic production of parathyroid hormone by small cell lung cancer in a patient with hiipofosfatemia. Coexisting hyperparathyroidism with familar. Hereditary hyperparathyroidism and multiple ossifying jaw fibromas: Raio X de joelhos apresentando exuberante calcinose bilateralmente.

Current Opinion in Rheumatology J Biol Chem ; Rev Bras Reumatol Autosomal dominant familial calcium pyrophosphate dihydrate deposition disease is caused by mutation in the transmembrane protein ANKH.


Raquitismo e osteomalácia hipofosfatêmicos de origem genética mediados por FGF

Hypercalcemia and ectopic secretion of parathyroid hormone by ovarian carcinoma with rearrangement of the gene for parathyroid hormone. Endocr Rev ;19 1: Localisation of a gene for chondrocalcinosis to chromosome 5p.

A parathyroid hormone-related protein implicated in maligant hypercalcemia: Condrocalcinose articular difusa CCAD. Hypercalcaemia caused by all-trans retinoic acid treatment of acute promyelocytic leukaemia: Hlpofosfatemia J Hum Genet ; A clinically and genetically distinct syndrome.

Hypercalcemia can less frequently be associated with some endocrine diseases like thyrotoxicosis, pheochromocytoma, Addison’s disease and multiple endocrine neoplasia types I and IIA. Serum levels of free 1,dihydroxyvitamin D in vitamin D toxicity. Transforming growth factor b increases stability of parathyroid hormone-related protein messenger RNA.

Alterations in transforming familiag factor-alpha and -beta production and cell responsiveness during the progression of MCF-7 human breast cancer cells to estrogen-autonomous growth. Therapy with colchicine was enough to prevent arthritic crisis in two patients and continous NSAID use was necessary to control symptoms in the last one.