artrogrypóza [Arthrogryposis]

tematický
31
Termíny

amyoplasia congenita
arthrogryposis multiplex congenita
arthrogryposis universalis congenita
syndrom mnohočetných kloubních kontraktur

 

Amyoplasia Congenita
Arthrogryposis Multiplex Congenita
Arthrogryposis Multiplex Congenita (AMC)
Arthromyodysplasia, Congenital
Congenital Arthromyodysplasia
Congenital Multiple Arthrogryposis
Fibrous Ankylosis of Multiple Joints
Guerin-Stern Syndrome
Guérin-Stern Syndrome
Myodystrophia Fetalis Deformans
Otto Syndrome
Rocher-Sheldon Syndrome
Rossi Syndrome

Perzistentní odkaz   https://www.medvik.cz/link/D001176
Definice

Termín používaný pro mnohočetné kongenitální svalové kontraktury. Tento příznak doprovází řadu neurologických onemocnění např. primární myopatie, virové myozitidy, infantilní spinální svalové atrofie aj.(cit. Velký lékařský slovník online, 2017 http://lekarske.slovniky.cz)

Persistent flexure or contracture of a joint.

Anotace
"persistent flexure or contracture of a joint"; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
DUI
D001176 MeSH Prohlížeč
CUI
M0001754
Historická pozn.
65(63)
Veřejná pozn.
65

C Nemoci
C05.550 nemoci kloubů 1 253
C05.550.069 ankylóza 65
C05.550.091 artralgie 275
C05.550.114 artritida 826
C05.550.150 artrogrypóza 31
C05.550.251 burzitida 57
C05.550.323 kontraktura 154
C05.550.445 hallux limitus 2
C05.550.450 hallux rigidus 26
C05.550.459 hemartróza 63
C05.550.509 hydrartróza 2
C05.550.518 dislokace kloubu 377
C05.550.521 nestabilita kloubu 252
C05.550.535 kloubní myšky 4
C05.550.610 metatarzalgie 12
C05.550.870 synovitida 172
C05.651 nemoci svalů 553
C05.651.102 artrogrypóza 31
C05.651.180 kompartment syndrom 113
C05.651.197 kontraktura 154
C05.651.324 fibromyalgie 133
C05.651.392 Isaacsův syndrom 7
C05.651.475 svalové křeče 176
C05.651.494 nádory svalů 17
C05.651.504 svalová rigidita 47
C05.651.512 svalová spasticita 457
C05.651.515 svalová slabost 224
C05.651.534 svalové atrofie 45
C05.651.542 myalgie 53
C05.651.594 myozitida 250
C05.651.662 myotonické poruchy 23
C05.651.682 myotoxicita 1
C05.651.742 polymyalgia rheumatica 110
C05.651.807 rhabdomyolýza 128
C05.651.869 tendinopatie 90
C05.660.077 artrogrypóza 31
C05.660.386 hrudník vpáčený 38
C05.660.417 gastroschiza 28
C05.660.745 pectus carinatum 1
C05.660.906 synostóza 29
C16.131 vrozené vady 1 741
C16.131.621.077 artrogrypóza 31
C16.131.621.142 kampomelická dysplazie 1
C16.131.621.174 syndrom krčního žebra 5
C16.131.621.386 hrudník vpáčený 38
C16.131.621.417 gastroschiza 28
C16.131.621.445 Hajdu-Cheney syndrom 6
C16.131.621.568 laryngomalacie 6
C16.131.621.585 vrozené deformity končetin 125
C16.131.621.745 pectus carinatum 1
C16.131.621.906 synostóza 29
C16.131.621.953 tracheobronchomalacie 9

Arthrogryposis and ectodermal dysplasia Disease MeSH Prohlížeč

Arthrogryposis epileptic seizures migrational brain disorder Disease MeSH Prohlížeč

Arthrogryposis multiplex congenita neurogenic type Disease MeSH Prohlížeč

Arthrogryposis multiplex congenita whistling face Disease MeSH Prohlížeč

Arthrogryposis multiplex congenita, distal type 1 Disease MeSH Prohlížeč

Arthrogryposis multiplex congenita, distal type 2 Disease MeSH Prohlížeč

Arthrogryposis multiplex congenita, distal, X-linked Disease MeSH Prohlížeč

Arthrogryposis multiplex with deafness, inguinal hernias, and early death Disease MeSH Prohlížeč

Arthrogryposis renal dysfunction cholestasis syndrome Disease MeSH Prohlížeč

Arthrogryposis, Distal, Type 10 Disease MeSH Prohlížeč

Arthrogryposis, Distal, Type 4 Disease MeSH Prohlížeč

Arthrogryposis, Distal, with Mental Retardation and Characteristic Facies Disease MeSH Prohlížeč

Arthrogryposis, X-Linked, Type V Disease MeSH Prohlížeč

Arthrogryposis, distal, type 2E Disease MeSH Prohlížeč

Arthrogryposis, distal, with hypopituitarism, mental retardation, and facial anomalies Disease MeSH Prohlížeč

Arthrogryposis-like hand anomaly and sensorineural deafness Disease MeSH Prohlížeč

Boylan Dew Greco syndrome Disease MeSH Prohlížeč

Bruck syndrome 1 Disease MeSH Prohlížeč

Bruck syndrome 2 Disease MeSH Prohlížeč

Camptodactyly-ichthyosis syndrome Disease MeSH Prohlížeč

Cataract, Microcephaly, Arthrogryposis, Kyphosis Syndrome Disease MeSH Prohlížeč

Cerebrooculofacioskeletal Syndrome 2 Disease MeSH Prohlížeč

Cerebrooculofacioskeletal Syndrome 4 Disease MeSH Prohlížeč

Contractures ectodermal dysplasia cleft lip palate Disease MeSH Prohlížeč

Cyprus facial neuromusculoskeletal syndrome Disease MeSH Prohlížeč

Distal arthrogryposis Moore Weaver type Disease MeSH Prohlížeč

Distal arthrogryposis type 2B Disease MeSH Prohlížeč

German Syndrome Disease MeSH Prohlížeč

Gordon syndrome Disease MeSH Prohlížeč

Hecht syndrome Disease MeSH Prohlížeč

Holoprosencephaly with Fetal Akinesia-Hypokinesia Sequence Disease MeSH Prohlížeč

Jequier Kozlowski skeletal dysplasia Disease MeSH Prohlížeč

Johnston Aarons Schelley syndrome Disease MeSH Prohlížeč

Kuskokwim disease Disease MeSH Prohlížeč

Ladda Zonana Ramer syndrome Disease MeSH Prohlížeč

Lethal Arthrogryposis With Anterior Horn Cell Disease Disease MeSH Prohlížeč

Lethal Congenital Contracture Syndrome 2 Disease MeSH Prohlížeč

Lethal congenital contracture syndrome 1 Disease MeSH Prohlížeč

Massa Casaer Ceulemans syndrome Disease MeSH Prohlížeč

Minicore myopathy, antenatal onset, with arthrogryposis Disease MeSH Prohlížeč

Multiple Pterygium Syndrome, Autosomal Dominant Disease MeSH Prohlížeč

Muscular Dystrophy, Congenital, Producing Arthrogryposis Disease MeSH Prohlížeč

Neuropathy, congenital, with arthrogryposis multiplex Disease MeSH Prohlížeč

Oculomelic amyoplasia Disease MeSH Prohlížeč

Pelvic dysplasia arthrogryposis of lower limbs Disease MeSH Prohlížeč

Pena Shokeir syndrome, type 1 Disease MeSH Prohlížeč

Podder-Tolmie syndrome Disease MeSH Prohlížeč

Ray Peterson Scott syndrome Disease MeSH Prohlížeč

Spondylohypoplasia, arthrogryposis and popliteal pterygium Disease MeSH Prohlížeč

Spranger Schinzel Myers syndrome Disease MeSH Prohlížeč

Tomaculous neuropathy Disease MeSH Prohlížeč