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180 Possible Causes for Alkaline Phosphatase Increased, Osteogenesis Imperfecta

  • Bone Disorder

    […] that increasing alkaline phosphatase levels in the blood.[] Abstract A recessive form of severe osteogenesis imperfecta that is not caused by mutations in type I collagen has long been suspected.[] As expected, as serum calcium decreased, serum phosphate, alkaline phosphatase, fibroblast growth factor-23 (FGF-23), parathyroid hormone, and osteoprotegerin increased, as[]

  • Osteogenesis Imperfecta

    Blood calcium, phosphate, albumin, fasting urinary calcium/creatinine ratio, total serum alkaline phosphatase, and bone alkaline phosphatase were obtained at baseline and[] Osteogenesis imperfecta (OI) is a group of genetic disorders that mainly affect the bones. The term " osteogenesis imperfecta " means imperfect bone formation.[] Levels of biochemical markers of bone metabolism generally were within the reference range, but serum alkaline phosphatase and urinary collagen type I N-telopeptide excretion[]

  • 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[] Craniotabes is a softening of skull bones that is known to be associated with a variety of pathological conditions, including rickets, hypervitaminosis A, osteogenesis imperfecta[] Laboratory test showed severe hypocalcemia, elevated alkaline phosphatase, normal serum phosphorous, decreased 25(OH) cholecalciferol, increased intact parathyroid hormone[]

  • Fracture

    Osteogenesis imperfecta (OI) is a generalised connective tissue disorder associated with low bone mass, bone fragility and increased susceptibility to fractures.[] However, a fracture may also be the result of some medical conditions which weaken the bones, for example osteoporosis, some cancers, or osteogenesis imperfecta (also known[] imperfecta, where the fracture is then properly termed a pathologic fracture.[]

  • Osteoporosis

    Increased rates of osteoclastic bone resorption, measured by the level of collagen breakdown products, as well as increased bone formation, measured by bone-specific alkaline[] Osteogenesis imperfecta (OI) is an inherited bone disorder that causes fractures due to impaired production of collagen type I.[] Considering the lack of other osteogenesis imperfecta (OI) symptoms and signs, the patient's illness can be classified as mild.[]

  • Congenital Bile Acid Synthesis Defect Type 2

    Página 323 - Consistent linkage of dominantly inherited osteogenesis imperfecta to the type I collagen loci: COL1A1 and COL1A2. Am J Hum Genet 46:293-307. ‎[]

  • Hereditary Hyperphosphatasia

    Abstract Hereditary hyperphosphatasia is a rare bone disorder characterized by increased bone turnover, elevated alkaline phosphatase (ALP) and bone deformity.[] Imperfecta 511 Chapter 20 Sclerosing Bone Dysplasias 541 Chapter 21 Parathyroid Disorders 557 Chapter 22 Fibrous Dysplasia 589 Chapter 23 Nutritional Rickets 625 Chapter[] , respectively, in serum tissue nonspecific alkaline phosphatase activity.[]

  • Osteomalacia

    Renal dysfunction, hypophosphatemia and increased levels of bone alkaline phosphatase were found.[] Osteopetrosis Osteogenesis imperfecta Molecular genetics for diagnosis and family studies.[] See Also: osteoclasis osteoclast osteocope osteocyte osteogenesis osteogenesis imperfecta osteogenic osteoid osteology osteoma osteomalacia osteometry osteomyelitis osteopath[]

  • X-Linked Hypophosphatemia

    Paricalcitol decreased alkaline phosphatase activity in adults by 21% (no change with placebo, P .04).[] BACKGROUND: Health-related quality of life of adults with osteogenesis imperfecta (OI), fibrous dysplasia (FD) and X-linked hypophosphatemia (XLH) remains poorly described[] Imperfecta 511 Chapter 20 Sclerosing Bone Dysplasias 541 Chapter 21 Parathyroid Disorders 557 Chapter 22 Fibrous Dysplasia 589 Chapter 23 Nutritional Rickets 625 Chapter[]

  • Osteitis Fibrosa Cystica

    […] in alkaline phosphatase to 486 units/l.[] Deficiency in collagen type I osteopenia Describe the type I & II osteogenesis imperfecta.[] Review Topic QID: 3480 3 Decreased 1,25-(OH)2-vitamin D3 4 Increased alkaline phosphatase ML 4 Select Answer to see Preferred Response PREFERRED RESPONSE 1 Sorry, this question[]

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