| Eponyms in category: Hands and arms |
| 29
main and alternative
entries found.
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| Akroosteolyse Typ Marie-Léri (German) (Marie-Léri syndrome) |
| A syndrome of peculiar hand deformity caused by osteolysis of the articular surfaces of the fingers. |
| Athlete's foot |
| A Fungus infection of the foot. |
| De Quervain's disease |
| Chronic tenosynovitis due to a narrowing process in the tendon sheaths around abductor policis longus and extensor pollicis brevis muscles. |
| de Quervain's syndrome (De Quervain's disease) |
| Chronic tenosynovitis due to a narrowing process in the tendon sheaths around abductor policis longus and extensor pollicis brevis muscles. |
| de Quervain's tendinitis (De Quervain's disease) |
| Chronic tenosynovitis due to a narrowing process in the tendon sheaths around abductor policis longus and extensor pollicis brevis muscles. |
| Dupuytren's contracture |
| Contracture of palmar fascia causing the ring and little fingers to bend into the palm so that they cannot be extended. |
| Gerhardt’s disease (Mitchell's syndrome I) |
| An idiopathic paroxysmal vasodilation of peripheral vasculature marked by sudden onset of burning pain in the hands and feet, diminution of temperature sense, and occasional glossalgia and feeding difficulty. |
| Gerhardt’s syndrome (Mitchell's syndrome I) |
| An idiopathic paroxysmal vasodilation of peripheral vasculature marked by sudden onset of burning pain in the hands and feet, diminution of temperature sense, and occasional glossalgia and feeding difficulty. |
| Gorlin's syndrome (Papillon-Léage and Psaume syndrome) |
| A congenital syndrome characterised by orofacial and digital defects. |
| Gorlin-Psaume syndrome (Papillon-Léage and Psaume syndrome) |
| A congenital syndrome characterised by orofacial and digital defects. |
| Iso-Kikuchi syndrome |
| A hand abnormality. |
| 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. |
| Léri's sign |
| A pyramidal sign, or joint reflex seen in spastic hemiplegia. |
| 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. |
| Léri’s phenomenon (Léri's sign) |
| A pyramidal sign, or joint reflex seen in spastic hemiplegia. |
| Léri’s reflex (Léri's sign) |
| A pyramidal sign, or joint reflex seen in spastic hemiplegia. |
| Madelung's deformity |
| Idiopathic progressive curvature of the radius. |
| Madelung's subluxation (Madelung's deformity) |
| Idiopathic progressive curvature of the radius. |
| Marie-Léri syndrome |
| A syndrome of peculiar hand deformity caused by osteolysis of the articular surfaces of the fingers. |
| Marinesco's hand |
| Cold blue oedematous hand with lividity of the skin seen in neurological lesions such as syringomyelia.
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| Marinesco's sign (Marinesco's hand) |
| Cold blue oedematous hand with lividity of the skin seen in neurological lesions such as syringomyelia.
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| Marinesco's succulent hand (Marinesco's hand) |
| Cold blue oedematous hand with lividity of the skin seen in neurological lesions such as syringomyelia.
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| Mitchell's syndrome I |
| An idiopathic paroxysmal vasodilation of peripheral vasculature marked by sudden onset of burning pain in the hands and feet, diminution of temperature sense, and occasional glossalgia and feeding difficulty. |
| Mitchell’s disease (Mitchell's syndrome I) |
| An idiopathic paroxysmal vasodilation of peripheral vasculature marked by sudden onset of burning pain in the hands and feet, diminution of temperature sense, and occasional glossalgia and feeding difficulty. |
| Papillon-Léage and Psaume syndrome |
| A congenital syndrome characterised by orofacial and digital defects. |
| Psaume’s syndrome (Papillon-Léage and Psaume syndrome) |
| A congenital syndrome characterised by orofacial and digital defects. |
| Schinzel's syndrome II |
| A familiar syndrome of ulnar ray defects, hand abnormalities, microgentialism, delayed puberty, obesity, and anal atresia. |
| Weir Mitchell's disease (Mitchell's syndrome I) |
| An idiopathic paroxysmal vasodilation of peripheral vasculature marked by sudden onset of burning pain in the hands and feet, diminution of temperature sense, and occasional glossalgia and feeding difficulty. |
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