| CIHS | central infantile hypotonic syndrome |
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| 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... |
| EIEE | Early infantile epileptic encephalopathy |
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| IHPS | Infantile Hypertrophic Pyloric Stenosis |
| IM | Infantile Myofibromatosis |
| IRD | Infantile Refsum disease |
| INAD | Infantile neuroaxonal dystrophy |
| infantile myxoedema | <paediatrics> Stunted body growth and mental development appearing in the first years of life resulting the inappropriate development of the thymus gland or inadequate maternal intake of iodine during gestation. (27 Sep 1997) |
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| pituitary myxoedema | Myxoedema resulting from inadequate secretion of the thyrotropic hormone; commonly occurs in association with inadequate secretion of other anterior pituitary hormones. (05 Mar 2000) |
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| congenital myxoedema | Stunted body growth and mental development appearing in the first years of life resulting the inappropriate development of the thymus gland or inadequate maternal intake of iodine during gestation. (27 Sep 1997) |
| myxoedema | <endocrinology> A functional insufficiency of the thyroid gland, resulting in deficiency of thyroid hormone. A variety of severe physiological problems accompany the reduction in thyroid function and the clinical features are dry skin, coarse hair, intolerance to cold, cognitive impairment and slowing of the relaxation phase of deep tendon reflexes. Clinical features: dry, waxy type of swelling with abnormal deposits of mucin in the skin and other tissues. The skin becomes puffy around the eyes and on the cheeks and the face is dull and expressionless with thickened nose and lips. The congenital form of the disease is cretinism. Severe hypothyroidism usually as a result of autoimmunity to thyroglobulin. (20 Sep 2002) |
| myxoedema heart | The enlarged heart associated with untreated severe hypothyroidism, often accompanied by pericardial effusion; rare in modern medicine. (05 Mar 2000) |
| myxoedema voice | <otolaryngology> The forced, rough, raucous voice of subjects of myxoedema, probably due to myxoedematous thickening of the vocal folds. (05 Mar 2000) |
| pretibial myxoedema | circumscribed myxoedema |
| operative myxoedema | Myxoedema developing after thyroidectomy. (05 Mar 2000) |
| 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) |
| diffuse infantile familial sclerosis | <radiology> Dysmyelinating disease, autosomal recessive, usually presents by 1 yr, specific enzyme deficiency identified, rapid spontaneous nystagmus, poikilothermia Synonym: Krabbe leukodystrophy (12 Dec 1998) |
| infantile | Pertaining to an infant or to infancy. Origin: L. Infantilis (18 Nov 1997) |
| infantile acute haemorrhagic oedema of the skin | A generally benign form of cutaneous vasculitis, characterised by ecchymotic purpura, often in a cockade pattern, and inflammatory oedema in infants. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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