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Traducción y análisis de palabras por inteligencia artificial ChatGPT
En esta página puede obtener un análisis detallado de una palabra o frase, producido utilizando la mejor tecnología de inteligencia artificial hasta la fecha:
- cómo se usa la palabra
- frecuencia de uso
- se utiliza con más frecuencia en el habla oral o escrita
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- ejemplos de uso (varias frases con traducción)
- etimología
myotonia congenita - traducción al ruso
myotonia congenita
медицина
болезнь Томсена
врождённая миотония
arthrogryposis
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![[[Lee Pearson]], a ten-time [[Paralympic Games]] gold medallist born with arthrogryposis](https://commons.wikimedia.org/wiki/Special:FilePath/Lee Pearson, October 2008.jpg?width=200 "[[Lee Pearson]], a ten-time [[Paralympic Games]] gold medallist born with arthrogryposis")
CONGENITAL JOINT CONTRACTURE IN TWO OR MORE AREAS OF THE BODY
Arthrogryposis multiplex congenita; Arthrogryposis due to muscular dystrophy; Arthrogryposis Multiplex congenita due to muscular dystrophy; Arthrogryposis Multiplex due to muscular dystrophy; Arthrogryposis ectodermal dysplasia other anomalies; Arthrogryposis and ectodermal dysplasia; Arthrogryposis epileptic seizures migrational brain disorder; Arthrogryposis IUGR thoracic dystrophy; Arthrogryposis like disorder; Kuskokwim disease; Arthrogryposis like hand anomaly sensorineural; Arthrogryposis like hand anomaly sensorineural deafness; Arthrogryposis-like hand anomaly and sensorineural deafness; Arthrogryposis like hand anomaly and sensorineural deafness; Arthrogryposis, distal, type 6; Cote Adamopoulos Pantelakis syndrome; Trichooculodermovertebral syndrome; TODV syndrome; Alves syndrome; Van Bervliet syndrome; Arthrogryposis multiplex congenita CNS calcification; Arthrogryposis multiplex congenita distal; AMCD; Arthrogryposis multiplex congenita, distal, x-linked; AMCX1; Gordon Syndrome; Arthrogryposis multiplex congenita neurogenic type; AMCN; Arthrogryposis multiplex congenita pulmonary hypoplasia; Fetal akinesia sequence; Fetal akinesia deformation sequence; Arthrogryposis multiplex congenita-pulmonary hypoplasia; Pena-Shokeir syndrome, type 1; Pena-Shokeir syndrome, type I; Arthrogryposis multiplex congenita whistling face; Illum syndrome; Arthrogryposis multiplex congenita, distal type 1; AMCD1; Arthrogryposis, distal, type 1; Distal arthrogryposis, type 1; DA 1; Arthrogryposis multiplex congenita, distal type 2; Arthrogryposis, distal, type 2B; Arthrogryposis multiplex congenita, distal type 2B; Freeman-Sheldon syndrome variant; Arthrogryposis ophthalmoplegia retinopathy; Oculomelic amyoplasia; Arthrogryposis, distal, type 5; Arthrogryposis, distal, type IIB; Arthrogryposis with oculomotor limitation and electroretinal abnormalities; Arthrogryposis renal dysfunction cholestasis syndrome; Arthrogryposis spinal muscular atrophy; Sheldon Hall syndrome; Index rotation flap; Dorsal carpal wedge osteotomy; Congenital contracture; Cote–Adamopoulos–Pantelakis syndrome; Cote-Adamopoulos-Pantelakis syndrome; Distal arthrogryposis; Arthrogriposis; Sheldon–Hall syndrome; Arthrogryposis multiplex with deafness, inguinal hernias, and early death
медицина
артрогрипоз
congenital contracture
CONGENITAL JOINT CONTRACTURE IN TWO OR MORE AREAS OF THE BODY
Arthrogryposis multiplex congenita; Arthrogryposis due to muscular dystrophy; Arthrogryposis Multiplex congenita due to muscular dystrophy; Arthrogryposis Multiplex due to muscular dystrophy; Arthrogryposis ectodermal dysplasia other anomalies; Arthrogryposis and ectodermal dysplasia; Arthrogryposis epileptic seizures migrational brain disorder; Arthrogryposis IUGR thoracic dystrophy; Arthrogryposis like disorder; Kuskokwim disease; Arthrogryposis like hand anomaly sensorineural; Arthrogryposis like hand anomaly sensorineural deafness; Arthrogryposis-like hand anomaly and sensorineural deafness; Arthrogryposis like hand anomaly and sensorineural deafness; Arthrogryposis, distal, type 6; Cote Adamopoulos Pantelakis syndrome; Trichooculodermovertebral syndrome; TODV syndrome; Alves syndrome; Van Bervliet syndrome; Arthrogryposis multiplex congenita CNS calcification; Arthrogryposis multiplex congenita distal; AMCD; Arthrogryposis multiplex congenita, distal, x-linked; AMCX1; Gordon Syndrome; Arthrogryposis multiplex congenita neurogenic type; AMCN; Arthrogryposis multiplex congenita pulmonary hypoplasia; Fetal akinesia sequence; Fetal akinesia deformation sequence; Arthrogryposis multiplex congenita-pulmonary hypoplasia; Pena-Shokeir syndrome, type 1; Pena-Shokeir syndrome, type I; Arthrogryposis multiplex congenita whistling face; Illum syndrome; Arthrogryposis multiplex congenita, distal type 1; AMCD1; Arthrogryposis, distal, type 1; Distal arthrogryposis, type 1; DA 1; Arthrogryposis multiplex congenita, distal type 2; Arthrogryposis, distal, type 2B; Arthrogryposis multiplex congenita, distal type 2B; Freeman-Sheldon syndrome variant; Arthrogryposis ophthalmoplegia retinopathy; Oculomelic amyoplasia; Arthrogryposis, distal, type 5; Arthrogryposis, distal, type IIB; Arthrogryposis with oculomotor limitation and electroretinal abnormalities; Arthrogryposis renal dysfunction cholestasis syndrome; Arthrogryposis spinal muscular atrophy; Sheldon Hall syndrome; Index rotation flap; Dorsal carpal wedge osteotomy; Congenital contracture; Cote–Adamopoulos–Pantelakis syndrome; Cote-Adamopoulos-Pantelakis syndrome; Distal arthrogryposis; Arthrogriposis; Sheldon–Hall syndrome; Arthrogryposis multiplex with deafness, inguinal hernias, and early death
медицина
врождённая контрактура
Wikipedia
Myotonia congenita
Myotonia congenita is a congenital neuromuscular channelopathy that affects skeletal muscles (muscles used for movement). It is a genetic disorder.
