| Eponyms in category: Skeleton |
| 67
main and alternative
entries found.
|
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| Abbott's method (Edville Gerhardt Abbott) |
| Gradual straightening of scoliosis by using a series of plaster jackets.
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| Bakwin-Eiger syndrome |
| Hereditary skeletal dysplasia affecting both sexes with characteristic cortical hyperplasia, macrocrania and hyperphosphatasis. |
| Beemer type (Beemer's syndrome) |
| A rare congenital dwarfing skeletal dysplasia. |
| Beemer's syndrome |
| A rare congenital dwarfing skeletal dysplasia. |
| Bloch-Stauffer dyshormonal syndrome (Rothmund-Thomson syndrome) |
| A rare hereditary oculocutaneous disorder with erythema, marble skin, pigmentation, telangiectasia, congenital cataracts, defective nails and teeth, partial to total alopecia, short stature, and congenital bone defects. |
| Bloch-Stauffer syndrome (Rothmund-Thomson syndrome) |
| A rare hereditary oculocutaneous disorder with erythema, marble skin, pigmentation, telangiectasia, congenital cataracts, defective nails and teeth, partial to total alopecia, short stature, and congenital bone defects. |
| Caffey's syndrome I (Caffey-Silverman syndrome) |
| Probably familial disease of infants affecting skeleton and adjacent tissues. |
| Caffey-Silverman syndrome |
| Probably familial disease of infants affecting skeleton and adjacent tissues. |
| Caffey-Smyth syndrome (Caffey-Silverman syndrome) |
| Probably familial disease of infants affecting skeleton and adjacent tissues. |
| Cervenka’s syndrome (Pepper's syndrome) |
| An inherited disorder characterized by craniofacial anomalies, skeletal abnormalities, obesity, mental retardation, and myotonia; without short stature or hypogonadism. |
| Cohen's syndrome (Pepper's syndrome) |
| An inherited disorder characterized by craniofacial anomalies, skeletal abnormalities, obesity, mental retardation, and myotonia; without short stature or hypogonadism. |
| De Toni-Caffey syndrome (Caffey-Silverman syndrome) |
| Probably familial disease of infants affecting skeleton and adjacent tissues. |
| De Toni-Caffey-Silverman syndrome (Caffey-Silverman syndrome) |
| Probably familial disease of infants affecting skeleton and adjacent tissues. |
| De Toni-Silverman-Caffey syndrome (Caffey-Silverman syndrome) |
| Probably familial disease of infants affecting skeleton and adjacent tissues. |
| Eaton-McKusick syndrome (Werner's syndrome) |
| A rare anomaly characterised by short legs due to absence of the tibia bilaterally, polydactyly of hands and feet, absence of thumbs, reduced knee movements. |
| Fairbank's syndrome II |
| A syndrome in which short stature is associated with multiple other abnormalities of the skeleton. |
| Feil-Klippel syndrome (Klippel-Feil deformity) |
| Congenital anomaly characterized by a reduced number of cervical vertebrae or multiple hemivertebrae fused into a single osseous mass, producing a short and wide neck with limited motion. |
| Feuerstein-Mims syndrome (Schimmelpenning-Feuerstein-Mims syndrome) |
| A congenital syndrome of anomalies affecting multiple body systems, especially the skin, skeleton, eyes, and central nervous system. |
| Frias' syndrome |
| Distinct form of the multiple pterygium syndrome with ptosis and skeletal anomalies. |
| Grudzinski's osteochondropathy (Silfverskiöld's syndrome) |
| An unusual form of osteochondrodystrophy with skeletal defects. |
| Herrmann-Pallister syndrome |
| Malformation- and dysmorphy syndrome with the triad of dwarfism, mental retardation and skeletal anomalies. |
| Herrmann-Pallister-Opitz syndrome (Herrmann-Pallister syndrome) |
| Malformation- and dysmorphy syndrome with the triad of dwarfism, mental retardation and skeletal anomalies. |
| Jadassohn's nevus phakomatosis (Schimmelpenning-Feuerstein-Mims syndrome) |
| A congenital syndrome of anomalies affecting multiple body systems, especially the skin, skeleton, eyes, and central nervous system. |
| Juvenile Paget's disease (Bakwin-Eiger syndrome) |
| Hereditary skeletal dysplasia affecting both sexes with characteristic cortical hyperplasia, macrocrania and hyperphosphatasis. |
| KBG syndrome (Herrmann-Pallister syndrome) |
| Malformation- and dysmorphy syndrome with the triad of dwarfism, mental retardation and skeletal anomalies. |
| Klippel's deformity |
| Congenital high position of the scapula in association with other anomalies of vertebrae and ribs.
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| Klippel-Feil anomalad (Klippel-Feil deformity) |
| Congenital anomaly characterized by a reduced number of cervical vertebrae or multiple hemivertebrae fused into a single osseous mass, producing a short and wide neck with limited motion. |
| Klippel-Feil deformity |
| Congenital anomaly characterized by a reduced number of cervical vertebrae or multiple hemivertebrae fused into a single osseous mass, producing a short and wide neck with limited motion. |
| Klippel-Feil phenotype (Klippel-Feil deformity) |
| Congenital anomaly characterized by a reduced number of cervical vertebrae or multiple hemivertebrae fused into a single osseous mass, producing a short and wide neck with limited motion. |
| Klippel-Feil syndrome (Klippel-Feil deformity) |
| Congenital anomaly characterized by a reduced number of cervical vertebrae or multiple hemivertebrae fused into a single osseous mass, producing a short and wide neck with limited motion. |
| Koslowski's syndrome |
| Polish paediatric radiologist, born June 6, 1928, Poznan.
His name is also spelled Koslowsky.
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| Koslowski-Maroteaux-Spranger syndrome (Koslowski's syndrome) |
| Polish paediatric radiologist, born June 6, 1928, Poznan.
His name is also spelled Koslowsky.
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| Koslowsky's type of chondrodysplasia (Koslowski's syndrome) |
| Polish paediatric radiologist, born June 6, 1928, Poznan.
His name is also spelled Koslowsky.
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| Kozlowski's spondylometaphyseal dysplasia syndrome (Koslowski's syndrome) |
| Polish paediatric radiologist, born June 6, 1928, Poznan.
His name is also spelled Koslowsky.
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| Lamy-Bienefeld syndrome (Léri-Weill syndrome) |
| A skeletal dysplasia combining dorsal subluxation of the distal end of the ulna (Madelung deformity) with mesomelic short stature. |
| Larsen’s syndrome (Rotter-Erb syndrome) |
| A skeletal dysplasia combining deformities of the bones, joints, and tendons. |
| Léri-Weill mesomelic dwarfism (Léri-Weill syndrome) |
| A skeletal dysplasia combining dorsal subluxation of the distal end of the ulna (Madelung deformity) with mesomelic short stature. |
| Léri-Weill syndrome |
| A skeletal dysplasia combining dorsal subluxation of the distal end of the ulna (Madelung deformity) with mesomelic short stature. |
| Lightwood and Payne idiopathic hypercalcaemia |
| A syndrome in infants. Only French description avialable. |
| McFarland’s syndrome (Rotter-Erb syndrome) |
| A skeletal dysplasia combining deformities of the bones, joints, and tendons. |
| Morquio-Silfverskiöld syndrome (Silfverskiöld's syndrome) |
| An unusual form of osteochondrodystrophy with skeletal defects. |
| Morquio’s variant syndrome (Silfverskiöld's syndrome) |
| An unusual form of osteochondrodystrophy with skeletal defects. |
| Otto-Chrobak disease (Otto-Chrobak pelvis) |
| Protrusion of the acetabulum into the pelvic cavity. |
| Otto-Chrobak pelvis |
| Protrusion of the acetabulum into the pelvic cavity. |
| Otto’s disease (Otto-Chrobak pelvis) |
| Protrusion of the acetabulum into the pelvic cavity. |
| Otto’s pelvis (Otto-Chrobak pelvis) |
| Protrusion of the acetabulum into the pelvic cavity. |
| Otto’s pelvis deformity (Otto-Chrobak pelvis) |
| Protrusion of the acetabulum into the pelvic cavity. |
| Pepper's syndrome |
| An inherited disorder characterized by craniofacial anomalies, skeletal abnormalities, obesity, mental retardation, and myotonia; without short stature or hypogonadism. |
| Roske-De Toni-Caffey syndrome (Caffey-Silverman syndrome) |
| Probably familial disease of infants affecting skeleton and adjacent tissues. |
| Roske-De Toni-Caffey-Silverman syndrome (Caffey-Silverman syndrome) |
| Probably familial disease of infants affecting skeleton and adjacent tissues. |
| Roske-De Toni-Caffey-Smyth syndrome (Caffey-Silverman syndrome) |
| Probably familial disease of infants affecting skeleton and adjacent tissues. |
| Rothmund dystrophy (Rothmund-Thomson syndrome) |
| A rare hereditary oculocutaneous disorder with erythema, marble skin, pigmentation, telangiectasia, congenital cataracts, defective nails and teeth, partial to total alopecia, short stature, and congenital bone defects. |
| Rothmund syndrome (Rothmund-Thomson syndrome) |
| A rare hereditary oculocutaneous disorder with erythema, marble skin, pigmentation, telangiectasia, congenital cataracts, defective nails and teeth, partial to total alopecia, short stature, and congenital bone defects. |
| Rothmund-Thomson syndrome |
| A rare hereditary oculocutaneous disorder with erythema, marble skin, pigmentation, telangiectasia, congenital cataracts, defective nails and teeth, partial to total alopecia, short stature, and congenital bone defects. |
| Rotter-Erb syndrome |
| A skeletal dysplasia combining deformities of the bones, joints, and tendons. |
| Saldino-Mainzer syndrome |
| A combination of renal dysplasia, pigment dystrophy of cornea, cerebellar ataxia, and skeletal dysplasia. |
| Schimmelpenning-Feuerstein-Mims syndrome |
| A congenital syndrome of anomalies affecting multiple body systems, especially the skin, skeleton, eyes, and central nervous system. |
| Schimmelpenning’s syndrome (Schimmelpenning-Feuerstein-Mims syndrome) |
| A congenital syndrome of anomalies affecting multiple body systems, especially the skin, skeleton, eyes, and central nervous system. |
| Silfverskiöld's syndrome |
| An unusual form of osteochondrodystrophy with skeletal defects. |
| Smyth-Caffey syndrome (Caffey-Silverman syndrome) |
| Probably familial disease of infants affecting skeleton and adjacent tissues. |
| Solomon's syndrome (Schimmelpenning-Feuerstein-Mims syndrome) |
| A congenital syndrome of anomalies affecting multiple body systems, especially the skin, skeleton, eyes, and central nervous system. |
| Solomon-Fretzin-Dewald syndrome (Schimmelpenning-Feuerstein-Mims syndrome) |
| A congenital syndrome of anomalies affecting multiple body systems, especially the skin, skeleton, eyes, and central nervous system. |
| Thomson-Rothmund syndrome (Rothmund-Thomson syndrome) |
| A rare hereditary oculocutaneous disorder with erythema, marble skin, pigmentation, telangiectasia, congenital cataracts, defective nails and teeth, partial to total alopecia, short stature, and congenital bone defects. |
| Werner's mesomelic dwarfism (Werner's syndrome) |
| A rare anomaly characterised by short legs due to absence of the tibia bilaterally, polydactyly of hands and feet, absence of thumbs, reduced knee movements. |
| Werner's syndrome |
| A rare anomaly characterised by short legs due to absence of the tibia bilaterally, polydactyly of hands and feet, absence of thumbs, reduced knee movements. |
| Wiedemann-Spranger disease |
| A very rare hereditary form of congenital skeletal dysplasia, of unknown aetiology and mode of transmission, characterized mainly by pseudorachitic long bone metaphyses and micromelic dwarfism. |
| Wiedemann-Spranger metaphyseal chondrodysplasia syndrome (Wiedemann-Spranger disease) |
| A very rare hereditary form of congenital skeletal dysplasia, of unknown aetiology and mode of transmission, characterized mainly by pseudorachitic long bone metaphyses and micromelic dwarfism. |
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