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74 Cards in this Set
- Front
- Back
the absence of fingers
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Adactyly
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Absence of upper, lower, or both limbs
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Amelia
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A feature of Marfan Syndrome
found in other disorders involoving genes that encode extracellular matrix proteins, such as Ehlers-Danlos syndrome |
Arachnodactyly
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Fusion of the fingers or toes caused by apoptosis of interdigital cells in fetal limb buds
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syndactyly
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hereditary condition in which the growth of long bones is retarded, resulting in short limbs
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Achondroplasia
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mutation of genes encoding chains of collagen type 1 and cause osteopenia
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Osteogenesis Imperfecta (OI)
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Caused by bone formation defects or pituitary abnormalities associated with growth hormone secretion
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Dwarfism
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Deficiency of GH receptor
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Laron-type dwarfism
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Deficiency of thyroid hormone
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cretinism
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Genetic disorder characterized by abnormal thickening of bones. AKA: Albers-Schonberg disease, marble bone disease
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Osteopetrosis
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"Lack of bone"
A decreased amount of bone visible on x-ray |
Osteopenia
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"Increase in porosity of bones"
A form of osteopenia characterized by decreased bone mass |
Osteoporosis
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age-related osteoporosis, accelerated bone loss
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Primary Osteoporosis
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Metabolic, endocrine, nutritional disorders causes this type of osteoporosis
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Secondary Osteoporosis
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"Softening of bones"
A metabolic disorder characterized by inadequate mineralization of osteoid |
Osteomalacia
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Osteomalacia in growing children
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Rickets
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Incresed bone resorption and replacement of bone trabeculae with fibrous tissue
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Hyperthyroidism
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Used to describe a set of changes seen in the bones of patients suffering from chronic renal insufficiency
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Renal osteodystrophy
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A disease of unknown etiology, characterized by abnormal remodeling and thickening of bones. AKA osteitis deformans
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Paget disease
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A stage of bone fracture healing which forms during the first week after fracture and is composed of granulation tissue, newly formed cartilage, and osteiod
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Provisional callus (procallus)
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A stage in bone fracture healing which during the 2nd week after fracture, it consists of more abudant collagenous matrix, cartilage, and osteoid in the process of calcification
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Fibrocartilginous callus
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A stage in bone fracture healing which is composed of haphazardly arranged bone spicules surrounded by CT
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Fibroosseous callus
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localized death of bone due to infarcts
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Osteonecrosis
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osteonecrosis of the head of the femur, typically found in 3-10 yr old boys
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Legg-Calve-Perthes disease
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osteonecrosis of the epiphysial tubercle of the tibia
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Osgood-Schlatter disease
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Inflammation of bones, most often caused by bacteria
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Osteomyelitis
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Chronic bone abscess fully enclosed by sclerotic bone
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Brodie Abscess
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osteomyelitis involving the vertebral column
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Pott disease
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the production of serum amyloid-associated protein which is deposited in the kidneys, liver, blood vessels, and other sites. Stimulated by chronic osteomyelitis
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amyloidosis
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Tumors of childhood and adolescence and involves the diaphysis of long bones
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Ewing sarcoma
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Tumors predominantly in the long bones of the extremities
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osteosarcoma
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Tumors that tend to involve the axial skeleton of the body
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chondrosarcomas
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Tumors the tend to occur in the metaphysis of long bones
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osteosarcomas
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The most common site of origin of giant cell tumors of the bone
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Epiphysis of long bones
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the most common malignant tumore of the metaphysis of long bones
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osteosarcoma
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The most common tumor of the diaphysis of long bones in children
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Ewing's sarcoma
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A small outgrowth of bone capped with cartilage and the most common benign tumor of bones
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osteochondroma
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the most common bone tumors of short bones of hands and feet
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Enchondromas
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one-sided enchondromas
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Ollier's Disease
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Multiple enchondromas associated with multiple hemangiomas
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Maffucci Syndrome
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Solitary benign bone tumors of the head of bones
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Osteomas
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Associated with colonic polyps in familial Gardner syndrome
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Osteomas
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fibroblastc tumors originating in the subperiosteal cortex of the metaphysis of long bones
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nonossifying fibromas
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the most common primary bone tumor, occuring in the metaphysis of long bones, and ~60% of all cases found in knee joint
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osteosarcomas
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bone tumor that invades locally and metatasizes hematogenously to the lung and is very malignant
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osteosarcoma
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2nd most common primary malignant bone tumor, peak incidence in 40-60 yr olds
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chondrosarcoma
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Tumor composed of undifferentiated primitiave cells of uncertain histogenesis, peak incidence in 5-20 yr olds
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Ewing Sarcoma
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This tumor forms bone spicules that are visible on x-ray(sunburst appearance) and give a gritty texture on sectioning
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osteosarcoma
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This bone tumor has "onion skin" appearance on x-ray
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Ewing sarcoma
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Benign tumor composed of spindle-shaped mononuclear cells, account for 20% of all bone tumors, peak incidence is 20-40 yrs old
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Giant cell tumor
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Most common malignant tumors metastasizing to the bones of adults
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Carcinomas of prostate, breast, lung, kidney, GI tract, thyroid
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tumor that presents with multiple lytic lesions, most prominent in the skull bone, ribs, and vertebrae
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multiple myeloma
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most common bone tumor in children and young people, originates from metaphysis of long bones
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osteosarcoma
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most common malignant bone tumor of adults, in axial skeleton
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chondrosarcoma
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A chronic disease characterized by progressive degneration, destruction, and loss of articular cartilage. AKA: DJD
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osteoarthritis
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osteophytes in distal interphalangeal DJD (1st carpometacarpal and 1st tarsometatarsal joints)
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Heberden node
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Chronic systemic disease of unknown etiology causing inflammation of diarthrodial joints
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Rheumatoid arthritis (RA)
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RA that begins before the age of 16
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Juvenille RA
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Diseases that involve the joints of the vertebral column
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spondyloarthropathy
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freely moveable joints held together by a joint capsule
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diarthrodial
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Seronegative arthropathy preferentially involving the vertebral column and sacrum
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ankylosing spondylitis
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Type of osteoporosis that primarily affects bones with large cancellous compartment, such as vertebral bodies. AKA postmenopausal
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Type 1 primary
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Osteoporosis that leads to thining of the cortical portion of long bones. AKA senile
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Type 2 primary
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an autoimmune condition that develops in response to an infection in another part of the body. AKA Reactive arthritis
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Reiter's syndrome
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A syndrome that includes a clinical triad of seronegative arthritis of large joints, urethritis, conjunctivitis
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Reiter syndrome
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evolves due to the extension of infections from adjacent structures or hematogenous spread
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infectious arthritis
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villous outgrowth of intraarticular synovial fronds that fill the joint cavity and consist of proliferating synovial lining cells, fibroblasts, angioblasts, and hemosiderin-laden macrophages and causes brownish color lesion
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pigmented villonodular synovitis
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A metabolic disease characterized by hyperuricemia and depostition of urate crystals in joints, subcutaneous soft tissue, and kidneys
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Gout
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idiopathic gout and accounts for 90% of all cases
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primary gout
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Gout which is a complication of other diseases or their treatment
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secondary gout
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overproduction of uric acid from nucleic acids
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hyperuricemia
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results from massive aggregates of uric acids, which form nodular masses protruding into joint and eroding the joint surfaces of the bones
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chronic tophaceous gout
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aggregates of urate crystals surrounded by infiltrates of lymphocytes and occurs most often in subperiosteal parts of the bones
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tophus
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A common joint disease caused by deposition of calcium pyrophosphate dihydrate (CPPD) crystals. AKA chondrocalcinosis
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psudogout
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