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637 Possible Causes for Osteoporosis, Osteosclerosis

  • Gaucher Disease

    In patients with symptomatic bone disease, lytic lesions can develop in the long bones, ribs, and pelvis, and osteosclerosis or osteopenia may be evident at an early age.[] Type 1 Gaucher disease (GD1) is characterized by thrombocytopenia, anemia, an enlarged spleen, and liver as well as bone complications (Erlenmeyer flask deformity, osteoporosis[] With regard to the skeletal status, all patients were negative for both osteosclerosis and osteonecrosis at baseline and week 24.[]

  • Pyknodysostosis

    Cathepsin K inhibitors will be useful in pathological processes involving excess osteoclast activation and bone resorption such as osteoporosis, bone metastasis and multiple[] Abstract Pyknodysostosis is an autosomal-recessive disorder of osteoclast dysfunction causing osteosclerosis, with associated maxillofacial anomalies.[] These findings suggest that cathepsin K is a major protease in bone resorption, providing a possible rationale for the treatment of disorders such as osteoporosis and certain[]

  • Renal Osteodystrophy

    He then developed a diffuse bone disease with osteosclerosis and roentgenographic features of hyperparathyroidism.[] Thus, CKD-related fractures can be considered a type of osteoporosis-where the bone quality is additionally impaired above that of age/hormonal-related osteoporosis.[] Effects on bone include osteosclerosis, osteomalacia, osteoporosis, pathologic fractures, aseptic necrosis of the hips, and bone pain.[]

  • Osteosclerosis

    Osteosclerosis can be classified in accordance with the causative factor into acquired and hereditary. [2] [1] Types [ edit ] Acquired osteosclerosis [ edit ] Osteogenic bone[] Seventeen (32%) patients had osteopenia/osteoporosis and 30 (57%) had osteosclerosis.[] Osteoporosis and osteosclerosis in sickle cell/beta-thalassemia: the role of the RANKL/osteoprotegerin axis Haematologica January 2006 91: 813-816; doi: Abstract Bone mineral[]

  • Autosomal Dominant Osteosclerosis Type Worth

    Treatment - Osteosclerosis autosomal dominant Worth type Not supplied. Resources - Osteosclerosis autosomal dominant Worth type Not supplied.[] Marcus’ laboratory was a study site for many of the pivotal clinical trials in the osteoporosis field.[] How is Autosomal Dominant Osteosclerosis, Worth type Treated? There is no cure for Autosomal Dominant Osteosclerosis, Worth type, since it is a genetic condition.[]

  • Acquired Osteosclerosis

    Both patients have diffuse osteosclerosis.[] Current Osteoporosis Reports 4: 153–158.[] Abstract Hepatitis C-associated osteosclerosis (HCAO) is a rare sclerosing bone condition characterized by debilitating, predominantly lower extremity bone pain, accelerated[]

  • Osteoporosis-Oculocutaneous Hypopigmentation Syndrome

    Diagnosis - Osteoporosis oculocutaneous hypopigmentation syndrome Home medical testing related to Osteoporosis - oculocutaneous - hypopigmentation syndrome: * Osteoporosis[] Osteosclerosis abnormalities of nervous system and meninges[?] Osteosclerosis autosomal dominant Worth type[?] Osteosclerosis[?] Ostertag type amyloidosis[?][] […] abnormalities of nervous system and meninges Osteosclerosis autosomal dominant Worth type Osteosclerosis Osteocytes Oster [ edit ] Ostertag type amyloidosis Ot–Ox [ edit[]

  • Systemic Mastocytosis

    Other cases of SM presenting as osteoporosis in male patients are also described.[] Bone manifestations of SM include: osteopenia with or without lytic lesions, osteoporosis with or without atraumatic fracture, osteosclerosis with increased bone density,[] Demos, MD TABLE CAUSES OF ADULT OSTEOSCLEROSIS[]

  • Osteomesopyknosis

    […] the US and the International Osteoporosis Foundation.[] Symptoms - Axial osteosclerosis Causes - Axial osteosclerosis Prevention - Axial osteosclerosis Not supplied.[] Osteomesopyknosis is a rare, recently described autosomal dominant condition which is characterized by benign osteosclerosis restricted to the axial skeleton (Simon et al,[]

  • Osteopetrosis

    Current Osteoporosis Reports 4: 153–158.[] This chapter deals with osteopetrosis (Albers–Schönberg marble bone disease), and pyknodyostosis due to defects in the acidification machinery of the osteoclasts; and osteosclerosis[] ARO caused by homozygous (or compound heterozygous) mutations in CLCN7, as described here, is usually diagnosed at birth or early in infancy due to generalized osteosclerosis[]

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