Magyar | Svéd orvosi |
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Löffler-szindróma [eosinophyl pneumonia] infoLöffler's syndrome, a disease in which eosinophils accumulate in the lung in response to a parasitic infection | Löffler syndrominfoakut eosinofil lunginfiltrat |
Miescher-szindróma II. [öröklődő acanthosis nigricans és diabetes mellitus együttesen] infoMiescher syndrome II, acanthosis nigricans in hereditary syndromes | Miescher-syndrom -et - [II.] |
Recklinghausen-szindróma II infotype 2 Recklinghausen disease, bilateral acoustic neurofibromatosis, vestibular schwannoma neurofibromatosis, or central neurofibromatosis | Recklinghausen-syndrom -et - [II.] |
Löffler-endocarditis [endocarditis eosinophilia fibroplastica Löffler] infoLöffler-endocarditis, restrictive cardiomyopathy, defined as an impaired relaxation of the heart with impaired diastolic filling | endokardit Löffler |
hangulati szindróma infomood disorder, a class of serious mental illnesses | förstämningssyndrom -et - |
Lobstein-szindróma infoLobstein's disease, Osteogenesis imperfecta, OI, a rare inherited disorder characterized by bone fragility and low bone mass | Lobstein-syndrom -et - |
Ritter-szindróma infoRitter disease, staphylococcal scalded skin syndrome, denudation of the skin | Ritter sjukdominfosmittosamt blåsutslag hos nyfödda |
Claude-szindróma [syndroma Claudei] infoClaude's syndrome, a form of brainstem stroke syndrome | Claude syndrominfonucleus ruber skada |
Maffucci-szindróma [enchondromatosis haemangiomával] [Maffucci syndroma] infoMaffucci syndrome, benign overgrowths of cartilage [enchondromas], skeletal deformities and cutaneous lesions composed of abnormal blood vessels | Kast syndrom |
lipodystrophia-szindróma [lipodystrophia intestinalis] infolipodystrophy syndrome, group of disorders characterized by either generalized or partial lack of adipose tissue | lipodystrofisyndrom -et - |
Haenel-szindróma [tabeses ocularis an[a]esthesia] infoHaenel symptom, absence of sensation on pressure of the eyeball in the tabes | Haenel symptominfoavsaknad av känsla på trycket i ögongloben i tabes |
Bäfverstedt-szindróma [P: Borrelial lymphocytoma] [lymphadenosis cutis benigna, morbus Bäfverstedti] infoBäfverstedt syndrome, pseudo-B-cell lymphoma of the skin | Bäfverstedt syndrominfoBäfverstedts sjukdom |
Scheie-szindróma infoScheie syndrome, a rare genetic lysosomal storage problem with an increased prevalence of carpal tunnel syndrome, CTS, in adolescence | Scheies syndrom |
Sly-szindróma [ß-glükuronidázhiány] infoshortage of beta-glucuronidase leads to a buildup of GAGs in the cells, specifically in the lysosomes | Slys sjukdominfomukopolysackaridos typ VII, MPS VII, beta-glukuronidasbrist |
Thiemann-szindróma [kéz- és lábujjak proximális interphalangealis ízületeinek avascularis nekrózisa] infoThiemann syndrome, avascular necrosis of the proximal interphalangeal joints of fingers and toes | Thiemann-syndrom -et - |
fusiós-szindróma infofusion syndrome, Klippel-Feil syndrome, a rare disorder where two or more vertebrae in the neck are fused together from birth | fusionssyndrom -et - |
Camera-szindróma [syndroma Camerai] infoCamera syndrome | Camera-syndrom -et - |
Edwards-szindróma [trisomia 18] infoEdwards syndrome, trisomy 18, having an extra chromosome 18 in some or all of the body's cells | Edwards syndrom |
Graefe-szindróma infovon Graefe's sign, the lagging of the upper eyelid on downward rotation of the eye, indicating exophthalmic goiter, Graves' disease | Graefe syndrom |
Turner-szindróma infoTurner syndrome, gonodal dysgenesis, a random genetic disorder that affects females | gonodal dysgenesi |
Volkmann-szindróma infoVolkmann's contracture, deformity of the hand, fingers, and wrist which occurs as a result of a trauma such as fractures, crush injuries, burns and arterial injuries | Volkmann syndrominfoförstörelse av muskler och kontrakturer pgavaskulära kompressio |
Foville-szindróma infoFoville syndrome | Fovilles syndrom |
Köhler-szindróma [osteochondrosis juvenilis ossis navicularis] infoKohler's disease, avascular necrosis, the navicular bone in the foot looses its blood supply temporarily and sustains a state of bone death | Köhlers sjukdom |
Aicardi-szindróma [syndroma Aicardisi] infomalformations in the brain, eyes and other parts of the body, Aicardis syndrome | Aicardis syndrominfoinfantila spasmer, okulära anomalier, agenesis av corpus callosum |
Avellis-szindróma [hemiparesis alternans vaga] infoAvellis syndrome, a peculiar form of alternating paralysis, spinothalamic tract-nucleus ambiguous syndrome | Avellis-syndrom -et - |
Bergman-szindróma [syndroma Bergmanus] [R] infoBergmann's syndrome, a cardio-oesophageal complex of symptoms in hiatus hernias in the diaphragm | Bergman syndrom |
Marshall-szindróma infoPFAPA, periodic fever, aphthous stomatitis, pharyngitis, adenitis, a childhood syndrome | PFAPA |
Heerfordt-szindróma [sarcoidosis] infoHeerfordt syndrome, a rare manifestation of sarcoidosis. The symptoms include inflammation of the eye [uveitis], swelling of the parotid gland | Heerfordt-syndrom -et - |
Morris-szindróma [férfi álhermafroditizmus] [feminisatio testicularis, endohermaphroditismus] infoMorris syndrome, X-linked recessive condition due to a complete or partial insensitivity to androgens, individuals with testes but of female phenotype | testikulär feminiseringinfoindivider med testiklar men av kvinnlig fenotyp |
Diamond-szindróma [P: Erysipelothrix rhusiopathiae] infoDiamond disease, swine erysipelas | Diamond-syndrom -et - |
Feer-szindróma [acrodynia] infoacrodynia, pain and dusky pink discoloration in the hands | akrodyni -n -erinfoupprepad exponering för kvicksilverföreningar hos barn |
Moebius-szindróma [f.r.] [congenitalis facialis diplegia] infoMoebius syndrome, congenital facial diplegia, associated with bilateral abducens nerve palsy | Möbius sekvensinfoavvikelser som har uppstatt till följd av en yttre orsak |
Tixier-szindróma [R] infoTixier syndrome, a fulminating haemolytic crisis in debilitated or malnourished newborns | Tixier-syndrom -et - |
Weber-szindróma infoWeber syndrome, occlusion of a branch of the posterior cerebral artery | Weber syndrominfopedunculus lesion som uppkommer till följd av ansikte, tunga och ögon muskelförlamning |
Stickler-szindróma infoStickler syndrome, hereditary progressive arthro-ophthalmopathy, a genetic disorder that can cause serious vision, hearing and joint problems | Sticklers syndrominfoär en i många fall ärftlig bindvävssjukdom som kan ge problem med hörsel, syn, skelett o. leder |
Kostmann-szindróma [congenital agranulocytosis] infoKostmann's syndrome, Kostmann syndrome, Kostmann disease, severe congenital neutropenia, SCN, infantile genetic agranulocytosis | Kostmanns sjukdom |
Lissauer-szindróma infoLissauer's general paresis | Lissauer syndrominfoatypiska progressiv förlamning |
Young-szindróma [férfi meddőség, bronchiectasis, sinusitis] infoYoung's syndrome, male infertility, damaged airways in the lungs [bronchiectasis], and inflammation of the sinuses [sinusitis] | Young-syndrom -et - |
Bouillaud-szindróma [arthritis rheumatica] infoBouillaud syndrome, rheumatic fever | Sokolsky-Bouillaud sjukdominforeumatoid artrit |
Eisenmenger-szindróma [f.r.] [Eisenmenger syndroma] infoEisenmenger syndrome, a long-term complication of an unrepaired heart problem present at birth | Eisenmengers syndrom |