| CIHS | central infantile hypotonic syndrome |
|---|---|
| CINCA | chronic infantile neurological cutaneous and auricular [syndrome] |
| EIEE | early infantile epileptic encephalopathy |
| FIMG | familial infantile myasthenia gravis |
| IA | ibotenic acid; immune adherence; immunoadsorbent; immunobiologic activity; impedance angle; indolami... |
| ADSD | Adductor spasmodic dysphonia |
|---|---|
| SD | Spasmodic dysphonia |
| ST | Spasmodic torticollis |
| TWSTRS | Toronto Western Spasmodic Torticollis Rating Scale |
| EIEE | Early infantile epileptic encephalopathy |
| spasmodic | Of the nature of a spasm. Origin: Gr. Spasmodes (18 Nov 1997) |
|---|---|
| spasmodic asthma | Asthma due to spasm of the bronchioles. (05 Mar 2000) |
| spasmodic dysmenorrhoea | Dysmenorrhoea accompanied by painful contractions of the uterus. (05 Mar 2000) |
| spasmodic dysphonia | Involves the muscles of the throat that control speech. Also called spastic dysphonia or laryngeal dystonia, it causes strained and difficult speaking or breathy and effortful speech. (12 Dec 1998) |
| spasmodic laryngitis | Catarrhal inflammation of the larynx in children, accompanied by night attacks of spasmodic closure of the glottis, causing inspiratory stridor. Synonym: spasmodic laryngitis. (05 Mar 2000) |
| spasmodic stricture | A stricture due to localised spasm of muscular fibres in the wall of the canal. Synonym: functional stricture, temporary stricture. (05 Mar 2000) |
| spasmodic tic | A disorder in which sudden spasmodic coordinated movements of certain muscles or groups of physiologically related muscles occur at irregular intervals. Synonym: Henoch's chorea. (05 Mar 2000) |
| spasmodic torticollis | A disorder of unknown cause, manifested as a restricted dystonia, localised to some of the neck muscles, especially the sternomastoid and trapezius; occurs in adults and tends to progress slowly; the head movements increase with standing and walking and decrease with contractual stimuli, e.g., touching the chin or neck. Synonym: dystonic torticollis, rotatory spasm, rotatory tic. (05 Mar 2000) |
| dysphonia, spasmodic | Involves the muscles of the throat that control speech. Also called spastic dysphonia or laryngeal dystonia, it causes strained and difficult speaking or breathy and effortful speech. (12 Dec 1998) |
| torticollis, spasmodic | Spasmodic torticollis, or torticollis, is the most common of the focal dystonias. In torticollis, the muscles in the neck that control the position of the head are affected, causing the head to twist and turn to one side. In addition, the head may be pulled forward or backward. Called wry neck. (12 Dec 1998) |
| aggressive infantile fibromatosis | A childhood counterpart of abdominal or extra-abdominal desmoid tumours, characterised by firm subcutaneous nodules that grow rapidly in any part of the body that invade locally and recur but do not metastasize. (05 Mar 2000) |
| autism, infantile | A syndrome beginning in infancy and characterised by a lack of responsiveness to other people, gross impairment in verbal and nonverbal communication skills, and bizarre responses to the environment. (12 Dec 1998) |
| progressive infantile spinal muscular atrophy | Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised. Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy. (05 Mar 2000) |
| spasms, infantile | Primary generalised epileptic seizures occurring in infants between birth and twelve months of age consisting of brief synchronous contractions of the neck, torso, and both arms. These seizures often occur in infants with underlying neurologic diseases. The prognosis for these infants is grave, with approximately ninety percent developing mental retardation in addition to their seizures. The eeg has a typical hypsarrhythmia pattern. The spasms and hypsarrhythmia have a tendency to disappear over the first three to five years of life, only to be replaced by other forms of generalised seizures. Infantile spasms sometimes respond to valproic acid or acth. (12 Dec 1998) |
| supravalvar aortic stenosis-infantile hypercalcaemia syndrome | <syndrome> Supravalvar aortic stenosis associated with elfin facies, mental retardation, and hypercalcaemia; usually sporadic; perhaps an irregular dominant trait. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|