UCSD Musculoskeletal Radiology bonepit.com Eponyms in MSK imaging |
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Adamkiewicz artery (373.) Addison disease (.545) Albright-Butler syndrome (.5723) Albright hereditary osteodystrophy (.534) Arnold-Chiari malformation (.1473) Takayasu (.625)Arthro-ophthalmopathy, hereditary (Stickler) (.1539) Sudeck (.499)
Baker cyst (.783) Beckwith-Wiedemann syndrome (.1719) Blount disease (.1481) Brodie abscess (cystic osteomyelitis) (.213), Buerger disease (.725) Burkitt lymphoma (.3435) (9.8347)
Caffey's disease Infantile cortical hyperostosis (Caffey) (.695) Caplan syndrome (pneumoconiosis with RhA) (.6114) Chance fracture (.419) Charcot Marie Tooth .8214 Chediak-Steinbrinck-Higashi syndrome (albinism, leukocyte inclusion, histiocytosis)(.2519) Chondroectodermal dysplasia (Ellis-van Creveld) (.1523) Chronic granulomatous disease of childhood (.2516) (Landing-Shirkey syndrome) (.296) Cockayne syndrome (dwarfism, retinal atrophy) (.1729) Coffin-Lowery syndrome (.1729) Congenital hyperuricemia (Lesch-Nyhan syndrome) (.599) Cornelia de Lange syndrome (dwarf, mental retardation) (.1723) Crohn disease arthritis with (.79)
Diamond-Blackfan syndrome (Triphalangeal thumb, red cell aplasia) (.653) Diffuse idiopathic skeletal hyperostosis (Forrestier disease) (.777) DiGeorge syndrome (absent parathyroids) (5.1966) (6.2514) DISH - see Diffuse idiopathic skeletal hyperostosis (Forrestier disease) (.777) Down syndrome (.184) Dupytrens contracture .3675 Dyggve-Melchior Clausen syndrome (.1529) Dyschondrosteosis (Leri Feil) (.1537) Dysplasia epiphysealis hemimelica (.1541),
Eagles syndrome .1390 Eagle-Barrett syndrome (.1444) Ehlers-Danlos syndrome (.1891) Ellis van Creveld syndrome (chondroectodermal dysplasia)(.1962) with hemangiomata (Maffucci) (1543) Engelmann disease (Camurati Engelmann, diaphyseal dysplasia) (.1555) Epiphyseal acrodysplasia (Thiemann) (.1538)
Fabry disease (.679) Fanconi anemia (radial ray) (.653) Fanconi syndrome (Renal tubular osteodystrophy) (.5723) Farber disease (disseminated lipogranulomatosis, joint swelling, erosions) (.679) Fong syndrome .1623 Forrestier disease (.777) in Cushing syndrome (.541) Freibergs infraction .4423
Galeazzi .4222 Gardner syndrome (4.3129) Gaucher disease (.67) Gorham disease (vanishing bone) (.3143) Gorlin syndrome (basal cell nevus syndrome) (.1671) Grebe syndrome (4.1511) (4.1629)
Hajdu-Chaney syndrome (.1861) Hand-Schuller-Christian disease (.662) Henoch purpura (.627) Hereditary arthro-ophthalmopathy (Stickler) (.1539) Hippel-Lindau syndrome (.1834) Holt-Oram syndrome (4.1641) Hunter syndrome (MPS II) (.1812) Hurler-Scheie compound (MPS I-H/S) (.1819) Hurler syndrome (MPS I-H) (.1811)
Infantile cortical hyperostosis (Caffey) (.695)
Jacoud arthritis (.79) Jaffe Campannacci .3131 Jansen type metaphyseal chondrodysplasia (.1536) Jarco Levine dysplasia (.1651) Jeune asphyxiating thoracic dysplasia (.1512) Juvenile kyphosis (Scheuermann disease) (.4963)
Kaposi sarcoma (.346) Kawasacki syndrome - see Mucocutaneous lymph node syndrome (.629) Kirner deformity (.1489) Klippel-Feil syndrome (.1432) Klippel-Trenaunay-Weber syndrome .3620 Kneist syndrome (.1526) Kozlowski type, spondylometaphyseal dysplasia (.1534) Kummel disease (.497)
Landing-Shirkey syndrome (granulomatous disease of childhood) (4.214) Langerhans cell histiocytosis (.66) Larsen syndrome (multiple congenital dislocations) (.1626) Laurence-Moon-Bardot-Biedel syndrome (syndactyly, mental retardation, obesity)(4.1894) Leri syndrome (pleonosteosis) (.1625) Leri Layani Weill syndrome (dyschondrosteosis) (.1537) Lesch-Nyhan syndrome (.599) Letterer-Siwe disease (.661)
Madelung defonmity (.1491) Marfan syndrome (.1711) (.1971) Marie-Strumpel disease (rhehmatoid spondylitis) (.8226) Maroteaux-Lamy syndrome (MPS VI) (.1815) McCune-Albright syndrome (polyostotic fibrous dysplasia) (.852) McKusick type metaphyseal chondrodysplasia (.1536) Menkes (kinky hair) syndrome (4.1726) Mesomelic dwarfism (Nievergelt, Langer, Robinow) (.1529) Meyer dysplasia (.134) Monteggia fx dis 422.4222 Morel Lavellee .4911 Morquio syndrome (MPS IV) (.1814) Morton neuroma .3645 Mueler Weiss .4416
Neimann-Pick disease (.672) .2551 Parsonage Turner Niemann-Pick disease (.67) (.672) Noonan syndrome (4.1642)
Osgood-Schlatter disease (4541.4490) Osteodysplasty (Melnick Needle syndrome) (.1559) Albright hereditary (.534)
Panner's disease .4422 Parsonage Turner syndrome .2551 Pellegrini-Stieda tendinitis (4514.2530) Perthes disease (.443) Pierre Robin anomaly (.1665) Poland syndrome (pectoral dysplasiadysdactyly) (.1621) Polyostotic fibrous dysplasia (McCune Albright) (.852) ischemic (aseptic) necrosis, Kummel disease (.497) with Raynaud phenomenon (.6131) Proteus syndrome .1835 Pseudo-Hurler polydystrophy (ML III) (.1823) Pyle disease (.1556)
Raynaud phenomenon, with progressive systemic sclerosis (.6131) Reticulum cell sarcoma-see Non-Hodgkin's lymphoma Ankylosing spondylitis (Marie-Strumpel disease) (.8226) Ridge syndrome (spondylosis) (.773) Riley Day syndrome .8212 Robert pseudo thalidomide syndrome (.1639) Rubenstein-Taybi syndrome (big thumbs, abnormal vertebrae) (.1622) Russell-Silver dwarfism (.1724)
Sandhoff disease (variant of Tay Sachs) (sphyngolipidosis)(.1829) Sanfilippo syndrome (MPS III) (.1813) Kaposi (.346) Scheie syndrome (MPS I-S) (.1819) Scheuermann disease (.4963) Schmid type metaphyseal chondrodysplasia (.1536) Schmorl node (.4961) Sjogren syndrome (.695) Smith-Lemli-Opitz syndrome (.1729) Sprengel deformity (.1485) Strudwick syndrome (.1527) Sturge-Weber syndrome (.1833) Sudeck atrophy (.565) Sulfatidosis, Austin type (.1829)
Tay-Sachs disease (.673) Treacher-Collins syndrome (.1664) Trichorhinophalangeal syndrome (Giedion) Trisomy 18 (Edward) (.1842) Trisomy 21 (Down) (.184) Turner syndrome (.1851)
Uhl anomaly (.1936)
Waldenstrom macroglobulinemia (.349) Wegener granulomatosis (.622) Weill-Marchesani syndrome (.1722) Werner syndrome (4.822) (7.7621) Whipple disease Wilson disease (4.789) (4.5729) Wilson-Mikity syndrome (.784) Winchester syndrome (.1869) Wiskott-Aldrich syndrome (.2513)
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