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591 Possible Causes for juvenile paget disease

  • Paget Disease of the Bone Type 5

    KEYWORDS: Alkaline phosphatase; Denosumab; Juvenile Paget disease; Osteoprotegerin; Receptor activator of nuclear factor-κB[ncbi.nlm.nih.gov] Juvenile Paget disease is rare; about 50 affected individuals have been identified worldwide. Juvenile Paget disease is caused by mutations in the TNFRSF11B gene.[ghr.nlm.nih.gov] Juvenile Paget disease is also known as osteoectasia with hyperphosphatasia, fragile bones and macrocranium, hyperostosis corticalis deformans juvenile, chronic idiopathic[roentgenrayreader.blogspot.com]

  • Hereditary Hyperphosphatasia

    Key-words Hypercalcemia juvenile Paget’s disease hyperphosphatasia post-partum APD This is a preview of subscription content, log in to check access.[link.springer.com] (OMIM phenotype number #239000 ) Familial hydiopatic hyperphosphatasia, also called juvenile Paget’s disease of bone, is a rare autosomal recessive juvenile-onset form of[iofbonehealth.org] Paget Disease of Bone 5, Juvenile-onset, PDB5 ; Online Mendelian Inheritance in Man (OMIM) Hofbauer LC, Schoppet M ; Osteoprotegerin deficiency and juvenile Paget's disease[patient.info]

  • Vitamin D Deficiency

    Juvenile Paget's disease (JPD) is a rare heritable osteopathy characterized biochemically by markedly increased serum alkaline phosphatase (ALP) activity emanating from generalized[ncbi.nlm.nih.gov]

  • Familial Paget Disease of Bone

    Mantzoros, Juvenile Paget disease, Metabolism, 10.1016/j.metabol.2017.10.007, (2017).[doi.org] Juvenile Paget's disease is a separate disease [ 3 ] - see separate Juvenile Paget's Disease article. See also separate Paget's Disease of Breast article.[patient.info] Autosomal recessive inheritance of deactivating mutations of the gene encoding OPG ( TNFRSF11B ) causes most cases of juvenile Paget disease.[doi.org]

  • Raynaud Phenomenon

    HIV & Rheumatic Diseases Hyperimmunoglobulin D Syndrome (Juvenile) Hypermobility (Juvenile) Inflammatory Myopathies Juvenile Arthritis Localized Scleroderma (Juvenile) Lupus[rheumatology.org] Lyme Disease Metabolic Myopathies Osteoarthritis Osteonecrosis Osteonecrosis of the Jaw (ONJ) Osteoporosis Paget's Disease of Bone Periodic Fever, Aphthous Stomatitis, Pharyngitis[rheumatology.org] Familial Mediterranean Fever (Juvenile) Fibromyalgia Giant Cell Arteritis Glucocorticoid-induced Osteoperosis Gout Granulomatosis with Polyangitis (Wegner's) HCV & Rheumatic Diseases[rheumatology.org]

  • Paget Disease of the Bone

    Autosomal recessive inheritance of deactivating mutations of the gene encoding OPG (TNFRSF11B) causes most cases of juvenile Paget disease.[ncbi.nlm.nih.gov] Juvenile Paget's disease is a separate disease [ 3 ] - see separate Juvenile Paget's Disease article. See also separate Paget's Disease of Breast article.[patient.info] Paget Disease of Bone 5, Juvenile-onset, PDB5 ; Online Mendelian Inheritance in Man (OMIM) Griz L, Fontan D, Mesquita P, et al ; Diagnosis and management of Paget's disease[patient.info]

  • Periostitis

    […] activation of RANK, and juvenile Paget's disease from OPG deficiency.[ncbi.nlm.nih.gov] Paget's disease, or Paget's disease of bone (PDB), respectively.[ncbi.nlm.nih.gov] Such conditions include familial expansile osteolysis, expansile skeletal hyperphosphatasia, and a familial form of early-onset Paget's disease of bone (PDB2), all from constitutive[ncbi.nlm.nih.gov]

  • Camurati-Engelmann Syndrome

    Disorders to consider include craniodiaphyseal dysplasia, autosomal dominant Kenny-Caffey syndrome, juvenile Paget disease, Ghosal hematodiaphyseal dysplasia, Worth type autosomal[orpha.net] Paget disease (OMIM 239000 ) TNFRSF11B AR Cranial hyperostosis, sensorineural hearing loss, sclerosis of long bones Predisposition to fractures, bowing of the long bones[ncbi.nlm.nih.gov] Differential diagnosis Camurati-Engelmann disease has characteristic clinical and radiological findings, reducing the need for extensive differential diagnosis.[orpha.net]

  • Prostate Sarcoma

    Grasemann et al (2013) stated that juvenile Paget's disease (JPD) is an extremely rare, yet painful and debilitating bone disease with onset occurring during early childhood[aetna.com] Juvenile Paget's disease can be caused by loss of function of osteoprotegerin (OPG), resulting in subsequent stimulation of osteoclasts via the RANK pathway.[aetna.com] Juvenile paget's disease in an Iranian kindred with vitamin D deficiency and novel homozygous TNFRSF11B mutation. J Bone Miner Res. 2013;28(6):1501-1508. Seton M.[aetna.com]

  • Prata-Libéral-Gonçalves Syndrome

    PEPCK deficiency, mitochondrial Pachyonychia congenita Jackson Lawler type Paes Whelan Modi syndrome Paget disease extramammary Paget disease juvenile type Paget's disease[mindmappedia.com] disease extramammary Paget disease juvenile type Paget's disease of bone Paget's disease of the breast Paget's disease, type 1 Pagon Bird Detter syndrome Pagon Stephan syndrome[bioreference.net] Paget disease extramammary[?] Paget disease juvenile type[?] Paget's disease of the breast[?] Paget's disease, type 1[?] Pagon Bird Detter syndrome[?][encyclopedia.kids.net.au]

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