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110 Cards in this Set
- Front
- Back
completely radiolucent
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Ameloblastoma
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commonly associated w/ impacted tooth (max canine)
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Adenomatoid Odontogenic Tumor (AOT
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loosening of teeth, uncommon, perio membrane origin
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Squamous Odontogenic Tumor
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Liesegang (lamellar) rings
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Calcifying Epithelial Odontogenic Tumor (CEOT)
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multilocular/honeycomb RL
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Odontogenic Myxoma
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rare, Max = ant to 1st molars, Mand = posterior to 1st molars. Non-specific RL.
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Central Odontogenic Fibroma
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Bump on gums
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Peripheral Odontogenic Fibroma
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teens – early 20’s à RADIOPAQUE mass of a VITAL tooth surrounded by a RADIOLUCENCENT ring
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Cementoblastoma
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RADIOPACITY +/- impacted tooth w/ RADIOLUCENCENT capsule
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Odontoma
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NON-aggressive odontogenic tumor affecting the mandibular molar-ramus area of children and young adults
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Ameloblastic Fibroma
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odontoma like radiopacities
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Ameloblstic Fibro-odontoma
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Malignant odontogenic tumors
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Primary intraosseous carcinoma (rare, high metastases)
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Malignant odontogenic tumors
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Ameloblastic carcinoma/malignant ameloblastoma (benign looking histo, but metastacises)
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Malignant odontogenic tumors
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Ameloblastic fibrosarcoma (mixed epithelial-mesenchymal w/ malignant mesenchymal)
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Malignant odontogenic tumors
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Clear cell odontogenic carcinoma (rare, clear cytoplasm, epithelial islands)
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Pericoronal unilocular
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name all
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Periapical unilocular
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name all
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Unilocular other locations
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name all
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Multilocular
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name all
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Mixed Radiolucent/opaque
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name all
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exaggerated lingual pit à early decay, tx: prophylactic fill. Permanent max laterals most common
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Dens in Dente (dens invaginatus):
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tubercle in center of occ table w/ pulp horn, relatively common. Bilateral PM's (Leung's) Asians, Inuits, Native Americans.
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Dens Evaginatus
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physologic(diet, occlusion
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Attrition
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pathologic(aggressive brushing, smoking/chewing tobacco),
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Abrasion
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chemical dissolution
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Erosion
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caused by environment + genetics
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Anodontia, polygenic
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abscessed primary tooth à pit formation
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Turner’s Tooth
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Fluorosis
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enamel hypoplasia
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Amelogenesis imperfecta 3 types
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hypocalcified, hypoplastic, hypomaturated
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bell shaped crowns
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Dentinogenesis Imperfecta
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chevron look
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Dentin dysplasia
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Ghost teeth
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Regional) Odontodysplasia
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No relation to inflammation trauma or systemic disease
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Pulpal Calcification
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pink tooth
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Internal Resorption
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may be caused by chronic inflammation, cysts, benign/malignant tumors, trauma, reimplantation, impaction, ortho, coronal resorption
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External Resorption
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green/brown primary teeth
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Erythroblastosis fetalis
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red/brown teeth
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Congenital porphyria
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apices of mandibular incisors, more common in Black females 20-30’s causing multiple radiolucent lesions of CITAL teeth
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Periapical cementoosseous dysplasia
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NOT in mandibular incisors, 90% women, RADIOLUCENT/mixed
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Focal cementoosseous dysplasia
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black women, multiquadrant +/- RADIOLUCENCIES, prone to osteomyelitis
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Florid cementoosseous dysplasia
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Slow expansion of jaws and craniofacial bones à well circumscribed defined border, mixed RL
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Ossifying fibroma
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mutation of GNAS1 Gene
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Fibrous dysplasia
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Ground Glass appearance
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Fibrous dysplasia
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Nocturnal pain (most others cause no pain) relieved by NSAIDs
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Osteoblastoma
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Multiple osteomas
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Gardner’s syndrome
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Benign proliferation of bone common in paranasal sinuses
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Osteoma
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area of increased bone density of unknown etiology = increased/well defined RP usually< 1cm, NOT associated with inflamed tooth.
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Ideopathic osteosclerosis aka dense bone island
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reaction due to chronic pulpal inflammation
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Condensing Osteitis aka focal sclerosing osteomyelitis
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Benign proliferation of multineuclated giant cells of jaws, most multilocular / some unilocular
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Central Giant Cell Granuloma
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soap bubble” +/- sun-ray-like appearance
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Hemangioma of Bone
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Can Mimic other intraosseous lesions
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Hemangioma of Bone
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Knees – teens, Jaws – 30’s
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Osteosarcoma
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elev serum alkaline phospatase, Histo: mosaic pattern, “reversal lines”, Radio: “cotton wool”
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Paget’s
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irreg wide PDL, “sun-ray”
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Osteosarcoma
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cartilage producing cells, rare, ant max
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Chondrosarcoma
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Young patients (children/teens), malignancy of bone
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Ewing’s Sarcoma/Primative Neuroectodermal Tumor:
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soft tissue variant of ewings sarcoma
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Primative Neuroectodermal Tumor
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Mult “punched out” RL – non-corticated
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Multiple Myeloma
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Malig plasma cell neoplasm
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Multiple Myeloma
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Single sight of bone destruction
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Solitary Plasmacytoma of Bone
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Jaw bones - ill-defined/subtle RL, alveolar bones lass, vague pain, parasthesia
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Non-Hodgkin Lymphomas
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Histo: “starry sky”
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Burkitt Lymphoma
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loose teeth, paresthesia
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Metastatic Dx
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Metastatic Dx to bones (primarily carcinoma) vs osteosarcoma in adults
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Metastatic Dx to bones (primarily carcinoma) > osteosarcoma in adults
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Young children, multiple osteolytic lesions of skull/jaw
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Langerhans Cell Histocytosis
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< one month duration, usually infectious, pain is primary Sx, NOT evident radiographically until 60% bone demineralized; purulent;
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Acute Osteomyeliti
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mild-moderate pain; NOTPurulent; moth-eaten radiographic appearance, mandibular molar MOST COMMON site, Swelling common
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Chronic Osteomyeliti
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Garre’s osteomyelitis
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Chronic osteomyelitis w/ proliferative periostiti
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associated w/ infected mandibular molar *ESP. in CHILDREN or as a post extraction complication; asymptomatic-mildly tender bony hard swelling w/ normal appearing overlying mucosa.
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Chronic osteomyelitis w/ proliferative periostiti
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onion skinning
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Chronic osteomyelitis w/ proliferative periostiti
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(looks like florid cementoosseus dysplasia
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Diffuse Sclerosing osteomyeliti
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condensing osteitis
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Focal Sclerosing osteomyeliti
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dry socket
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Alveolar Osteitis
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Radiation injury to bone 3 h's
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1. Hypovascular; 2. Hypocellular; 3. hypoxic
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delayed eruption/ supernumerary
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Cleidocranial dysplasia/Gardner/Crouzon
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delayed eruption/ missing teeth
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downs / osteopetrosis
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too few/too many teeth
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Ehlers-Danlos, Sturge Weber
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too few teeth
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Ectodermal dysplasia / Hurler
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premature exfoliation
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Papillon LeFevre, Hyphosphatasia, Dentinal dysplasia type 1, Regional odontodysplasia
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prolonged retention of primary teeth and eruption failure of permanent teeth and often exhibits supernumary teeth
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Cleidocranial dysplasia
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bilateral asymptomatic swelling of the jaws, upturned gaze, multilocular RL’s = giant cell lesions. Permanent teeth may be malformed or missing
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Cherubism
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Frog-like" facies
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Crouzon's Syndrome
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most common craniosynostosis syndromes
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Crouzon's and Apert’s
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Autosomal dominant, MULTIPLE - OKC's, basal cell carcinomas and epidermoid cysts. Palmar-plantar pitting. Large calvaria, Calcification of falx cerebri, bifid ribs, ovarian fibromas.
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Basal Cell Nevus Syndrome
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hypotrichosis (less than normal amount of hair on head), hypohydrosis, cone-shaped teeth. Heat intolerance
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Ectodermal Dysplasia
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deficiency of lysosomal enzymes
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Mucopolysaccharidoses
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Clinically evident by age two--patient usually dies by age 25 due to cardiopulmonary disease, short stature; hepatosplenomegaly; hernias normal mental capacity; sleep apnea-airway obstruction; corneal clouding Dysostosis multiplex; thickened skin; hearing loss (12%)
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Hurler-Scheie Syndrome
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CT disorder-defect [fibrillin (FBN1) gene]
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Marfan's Syndrome
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Fragile bones inborn error of collagen
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Osteogenesis Imperfecta
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Severe micrognathia, high palate, feeding problems
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Pierre Robin Syndrome
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bird-like or fish-like facies
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Treacher-Collins Syndrome
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mandibular hypoplasia; midface deficiency, colobomas (notches
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Treacher-Collins Syndrome
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rubber man
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Ehlers-Danlos Syndrome
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Joint hypermobility; skin hyperextensibility. Cardiovascular anomalies; possible bleeding problems, need antibiotic prophylaxis
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Ehlers-Danlos Syndrome
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Tall forehead with flattened occipital; premature suture closure, ocular proptosis with downward slant to corners of eye, mid-face hypoplasia; mouth breather (Class III with anterior open bite, syndactyly of fingers and toes, mental retardation; acne-like eruption on forearm, 75% soft palate cleft, bifid uvula, V-shaped arch; shovel shaped incisors; mucosal swellings.
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Apert's Syndrome
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Unilateral localized overgrowth of facial soft tissue, bones, and teeth
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Hemifacial Hypertrophy
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Opposite of Hemifacial Hypertrophy with localized scleroderma (hardening and thickening of skin
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Parry-Romberg Syndrome
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midface hypoplasia; delayed eruption, hypodontia and microdontia more common; fissured enlarged tongue; greater incidence of periodontal disease and infections; crossbite common; mouth-breathers, thyroid dysfunction in 50%, increased risk of ALL (leukemia), cardiac abnormalities
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Down syndrome
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Hyperkeratotic palms and soles, lack of resistance to periodontal disease; defective neutrophil chemotaxis à tooth loss within 2-3 years post-eruption No Tx
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Papillon-Lefevre Syndrome
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auriculo-temporal syndrome, following parotid surgery, trauma, mandibular surgery, parasympathetic nerve fibers may be severed à sweating, flushing, warmth, and occasional mild pain during enhanced salivary stimulation when eating food
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Frey syndrome
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PFAPA:
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Periodic fever, Aphthous ulcers, Pharyngitis, Cervical Adenitis in children
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Elevated serum alkaline phosphatase My hat doesn’t fit anymore
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Paget's Disease of Bone
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pituitary adenoma after puberty
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Acromegaly
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enlargment of the hands and feet
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Acromegaly
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deficiency of tissue and serum alkaline phosphatase, increases serum phosphoethanolamine, beaten copper skull appearance,premature loss of primary teeth (lack cementum),enlarged pulp chamber in primary teeth with alveolar bone loss, short stature, bowed legs, waddling gait
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Hypophosphatasia
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stones, moans, bones and groans
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Hyperparathyroidism
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parathyroid adenoma; secondary form due to renal failure
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Hyperparathyroidism
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Premature exfoliation of primary teeth or rapid eruption of permanent teeth dental erosion 3x as likely, osteoporosis, females 5:1; Grave's disease, heat intolerance, weight loss, hyperhydrosis, diarrhea, thin hair, exophthalmos
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Hyperthyroidism
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Grave's disease
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Hyperthyroidism
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Delayed dental development. Put on weight
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Hypothyroidism
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