¼±Åà - È­»ìǥŰ/¿£ÅÍŰ ´Ý±â - ESC

 
"DYS"¿¡ ´ëÇÑ ¼¼ºÎ °Ë»ö °á°úÀÔ´Ï´Ù
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 5 ÆäÀÌÁö: 6
  • Dystocia - »õâ Slow or difficult OBSTETRIC LABOR or CHILDBIRTH.
    Synonyms : Dystocias
  • Dystonia - »õâ A persistent attitude or posture due to the co-contraction of agonists and antagonist muscles in one region of the body. It most often affects the large axial muscles of the trunk and limb girdles. Conditions which feature persistent or recurrent episodes of dystonia as a primary manifestation of disease are referred to as DYSTONIC DISORDERS. (Adams et al., Principles of Neurology, 6th ed, p77)
    Synonyms : Dystonia, Diurnal, Dystonia, Limb, Dystonia, Paroxysmal, Diurnal Dystonia, Dystonia, Muscle, Limb Dystonia, Paroxysmal Dystonia
  • Dystonia Musculorum Deformans - »õâ A condition characterized by focal DYSTONIA that progresses to involuntary spasmodic contractions of the muscles of the legs, trunk, arms, and face. The hands are often spared, however, sustained axial and limb contractions may lead to a state where the body is grossly contorted. Onset is usually in the first or second decade. Familial patterns of inheritance, primarily autosomal dominant with incomplete penetrance, have been identified. (Adams et al., Principles of Neurology, 6th ed, p1078)
    Synonyms : Dystonia Deformans Musculorum, Dystonia Deformans Progressiva, Torsion Disease of Childhood, Dystonia, Idiopathic Torsion, Dystonias, Idiopathic Torsion, Dystonias, Torsion, Idiopathic Torsion Dystonias, Oppenheim Ziehen Disease, Spasm, Progressive Torsion
  • Dystonic Disorders - »õâ Acquired and inherited conditions that feature DYSTONIA as a primary manifestation of disease. These disorders are generally divided into generalized dystonias (e.g., dystonia musculorum deformans) and focal dystonias (e.g., writer's cramp). They are also classified by patterns of inheritance and by age of onset.
    Synonyms : Adult-Onset Dystonias, Adult-Onset Idiopathic Focal Dystonias, Adult-Onset Idiopathic Torsion Dystonias, Autosomal Dominant Familial Dystonia, Autosomal Recessive Familial Dystonia, Childhood Onset Dystonias, Dystonia Disorders, Dystonia, Hereditary
  • Dystroglycans - »õâ Dystrophin-associated proteins that play role in the formation of a transmembrane link between laminin-2 and DYSTROPHIN. Both the alpha and the beta subtypes of dystroglycan originate via POST-TRANSLATIONAL PROTEIN PROCESSING of a single precursor protein.
    Synonyms : Cranin, Dystrophin-Associated Glycoprotein 1, alpha-Dystroglycan, beta-Dystroglycan, dystroglycan 1, Dystrophin Associated Glycoprotein 1, alpha Dystroglycan, beta Dystroglycan
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
MeSH(Medical Subject Headings) À¯»ç °Ë»ö (http://www.nlm.nih.gov) °á°ú : 0 ÆäÀÌÁö: 6
ÅëÇÕ°Ë»ö ¿Ï·á