Tertiary hyperparathyroidism in a patient with X-linked hypophosphatemic rickets. 2011

S Tournis, and T Georgoulas, and C Zafeiris, and C Papalexis, and K Petraki, and G P Lyritis
Laboratory for Research of Musculoskeletal System Theodoros Garofalidis, KAT Hospital, University of Athens, Athens, Greece. stournis@med.uoa.gr

UI MeSH Term Description Entries
D006961 Hyperparathyroidism A condition of abnormally elevated output of PARATHYROID HORMONE (or PTH) triggering responses that increase blood CALCIUM. It is characterized by HYPERCALCEMIA and BONE RESORPTION, eventually leading to bone diseases. PRIMARY HYPERPARATHYROIDISM is caused by parathyroid HYPERPLASIA or PARATHYROID NEOPLASMS. SECONDARY HYPERPARATHYROIDISM is increased PTH secretion in response to HYPOCALCEMIA, usually caused by chronic KIDNEY DISEASES.
D009397 Nephrocalcinosis A condition characterized by calcification of the renal tissue itself. It is usually seen in distal RENAL TUBULAR ACIDOSIS with calcium deposition in the DISTAL KIDNEY TUBULES and the surrounding interstitium. Nephrocalcinosis causes RENAL INSUFFICIENCY. Nephrocalcinoses
D011859 Radiography Examination of any part of the body for diagnostic purposes by means of X-RAYS or GAMMA RAYS, recording the image on a sensitized surface (such as photographic film). Radiology, Diagnostic X-Ray,Roentgenography,X-Ray, Diagnostic,Diagnostic X-Ray,Diagnostic X-Ray Radiology,X-Ray Radiology, Diagnostic,Diagnostic X Ray,Diagnostic X Ray Radiology,Diagnostic X-Rays,Radiology, Diagnostic X Ray,X Ray Radiology, Diagnostic,X Ray, Diagnostic,X-Rays, Diagnostic
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults
D053098 Familial Hypophosphatemic Rickets A hereditary disorder characterized by HYPOPHOSPHATEMIA; RICKETS; OSTEOMALACIA; renal defects in phosphate reabsorption and vitamin D metabolism; and growth retardation. Autosomal and X-linked dominant and recessive variants have been reported. Hypophosphatemic Rickets, X-Linked Dominant,Rickets, X-Linked Hypophosphatemic,Generalized Resistance To 1,25-Dihydroxyvitamin D,Hereditary Hypophosphatemic Rickets,Hereditary Vitamin D-Resistant Rickets,Hypocalcemic Vitamin D-Resistant Rickets,Hypophosphatemia, X-Linked,Hypophosphatemic Rickets, X-Linked Recessive,Rickets, Hereditary Vitamin D-Resistant,Vitamin D-Resistant Rickets With End-Organ Unresponsiveness To 1,25-Dihydroxycholecalciferol,Vitamin D-Resistant Rickets, Hereditary,Vitamin D-Resistant Rickets, X-Linked,X-Linked Hypophosphatemia,Generalized Resistance To 1,25 Dihydroxyvitamin D,Hereditary Vitamin D Resistant Rickets,Hypocalcemic Vitamin D Resistant Rickets,Hypophosphatemia, X Linked,Hypophosphatemic Rickets, Familial,Hypophosphatemic Rickets, Hereditary,Hypophosphatemic Rickets, X Linked Dominant,Hypophosphatemic Rickets, X Linked Recessive,Hypophosphatemic Rickets, X-Linked,Rickets, Familial Hypophosphatemic,Rickets, Hereditary Hypophosphatemic,Rickets, Hereditary Vitamin D Resistant,Vitamin D Resistant Rickets With End Organ Unresponsiveness To 1,25 Dihydroxycholecalciferol,Vitamin D Resistant Rickets, Hereditary,Vitamin D Resistant Rickets, X Linked,X Linked Hypophosphatemia,X-Linked Hypophosphatemic Rickets
D040181 Genetic Diseases, X-Linked Genetic diseases that are linked to gene mutations on the X CHROMOSOME in humans (X CHROMOSOME, HUMAN) or the X CHROMOSOME in other species. Included here are animal models of human X-linked diseases. X-Linked Genetic Diseases,Genetic Diseases, X-Chromosome Linked,Disease, X-Linked Genetic,Diseases, X-Linked Genetic,Genetic Disease, X-Linked,Genetic Diseases, X Chromosome Linked,Genetic Diseases, X Linked,X Linked Genetic Diseases,X-Linked Genetic Disease

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