| 영문 | spinal tap, spinal puncture | 한글 | 허리천자, 요추천자, 요추뚫기 |
|---|---|---|---|
| 설명 | 질병의 진단이나 치료 또는 마취를 하기 위해 피부에서 거미막밑공간으로 바늘을 찌를 때가 있다. 이것은 셋째 허리뼈 아래쪽에서 시행한다. 척수가 첫째 허리뼈 아랫모서리에서 끝나고, 거미막밑공간은 둘째 엉치뼈 분절까지 뻗어 있기 때문에 이 부위는 바늘로 척수를 찌를 위험이 없다. 또 척추뼈고리판이 짧아 서로 겹쳐있지 않기 때문에 허리뼈 사이로 바늘을 찌를 수 있다. 이 부위의 거미막밑공간에는 척수신경 뿌리가 있으나, 이들은 뇌척수액속에 있기 때문에 바늘을 넣을 때 한쪽으로 밀려 손상받는 경우는 거의 없다. 배를 넓적다리에 붙일정도로 허리를 구부리면 고리판 사이가 더 벌어져 틈이 커진다. 바늘이 뚫고 지나가는 구조는 바깥에서 속으로 ① 피부, ② 피부밑조직, ③ 근육막, ④ 가시끝인대, ⑤ 가시사이인대, ⑥ 황색인대, ⑦ 경질막, ⑧ 거미막, ⑨ 뇌척수액이 된다.  |
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| 영문 | muscular system | 한글 | 근육계통 |
|---|---|---|---|
| 설명 | 근육에 의해 이루어진 하나의 계통을 임의적으로 나누어 부른 말. |
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| 영문 | muscular dystrophy | 한글 | 근육퇴행위축 |
|---|---|---|---|
| 설명 | 근섬유의 파괴로 인한 점진적인 근위축과 허약을 특징으로 하는 일련의 선천적인 질환군을 통털어 말한다. 대표적인 경우가 뒤쉔(Duchenne)형으로 성염색체 열성유전을 하며, 대개 4 세이내에 발병해 청년기를 넘기는 경우가 드물다. 특징적 소견으로 장딴지근(gastronemius)의 거짓비대(pseudohypertrophy)(실제적으로는 근위축이 일어나지만, 근섬유 대신에 지방세포가 들어차 도리어 마치 근육이 증가한 것처럼 보이는 현상) 소견을 볼 수 있다. |
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| 영문 | childhood diabetes | 한글 | 소아당뇨병 |
|---|---|---|---|
| 설명 | 소아에 나타나는 당뇨병. 당뇨병은 인슐린 부족으로 체내 포도당 이용이 저하되어 탄수화물-지방-단백질 대사가 장해를 일으키는 질병으로, 성인형 당뇨병과 연소형 당뇨병이 있다. 성인형은 인슐린의 상대적 부족, 즉 비만으로 인한 인슐린 감수성의 저하 결과 인슐린 필요량의 증대에서 오는 것이며, 소아형 당뇨병은 이자의 랑게르한스섬 베타(β)세포의 장해로 인한 인슐린의 절대적 결핍에서 온다. 세계보건기구(WHO)의 권장으로 15세 이전에 발병하는 당뇨병을 모두 소아당뇨병이라 하는데, 어린이에게도 간혹 성인형(또는 비만형) 당뇨병이 있으므로 소아당뇨병이라 함은 소아기에 발병하는 소아형과 성인형 당뇨병의 총칭이라 할 수 있다. 현재까지 통계에 의하면 전체인구의 약 5%는 당뇨병을 가지고 있으며, 그 가운데 약 2%가 15세 이전에 발병하는 것으로 알려졌다. |
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| 영문 | childhood | 한글 | 아동기, 소아기 |
|---|---|---|---|
| 설명 | 넓은 뜻으로는 출생에서부터 청년기에 들어가기 직전까지, 즉 12~13세경까지를 말한다. 육체적으로도 정신적으로도 성장발육하고 있는 시기의 인간을 총칭해서 어린이 혹은 소아라고 하며 이 시기를 말한다. 달력 연령에 따라서 출생 전기, 출생에서 4주간을 신생아기, 그 신생아기를 포함해서 생후 1년까지가 영아기, 생후 1년 이후부터 취학 전까지의 시기를 유아기, 취학 후부터 초등학교 졸업까지의 6~12세의 시기를 학동기, 여아에서는 10~18세까지, 남아에서는 12~20세까지를 사춘기라고 한다. |
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| CMD | campomelic dysplasia; camptomelic dwarfism; cartilage matrix deficiency; chief medical director; chi... |
|---|---|
| PMD | Progressive Muscular Dystrophy; 진행성 근이영양증 Types of PMD(Progressive Muscular Dystroph... |
| CSMA | chronic spinal muscular atrophy |
| FSHSMA | facioscapulohumeral spinal muscular atrophy |
| PSMA | proximal spinal muscular atrophy |
| SMA | Spinal muscular atrophies |
|---|---|
| SMAs | Spinal muscular atrophies |
| SCARMD | Severe childhood autosomal recessive muscular dystrophy |
| HCSMA | Hereditary Canine Spinal Muscular Atrophy |
| SMA | SPINAL muscular atrophy |
| childhood muscular dystrophy | The most common childhood muscular dystrophy, with onset usually before age 6. Characterised by symmetrical weakness and wasting of first the pelvic and crural muscles and then the pectoral and proximal upper extremity muscles; pseudohypertrophy of some muscles, especially the calf; heart involvement; sometimes mild mental retardation; progressive course and early death, usually in adolescence. X-linked inheritance (affects males and transmitted by females). Synonym: childhood muscular dystrophy, Duchenne's disease, pseudohypertrophic muscular dystrophy. (05 Mar 2000) |
|---|---|
| muscular atrophy, spinal | Progressive degenerative disorder of motor neurons in the spinal cord, brainstem, and motor cortex, manifested clinically by muscular weakness, atrophy, and corticospinal tract signs in varying combinations. (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) |
| progressive spinal muscular atrophy | One of the subgroups of motor neuron disease; a progressive degenerative disorder of the motor neurons of the spinal cord, manifested as progressive, often symmetrical, weakness and wasting, typically beginning in the distal portions of the limbs, particularly in the upper extremities, and spreading proximally; fasciculation potentials are often present, but evidence of corticospinal tract disease (e.g., increased deep tendon reflexes, Babinski sign) is not. (05 Mar 2000) |
| spinal muscular atrophy | <radiology> 2nd most common autosomal recessive disease in Caucasians, pathology, degeneration of the spinal anterior horn cells, atrophy and wasting of skeletal muscles, types, SMA I = Werdnig-Hoffman disease: rapidly progressive, SMA II = intermediate form, SMA III = Kugelberg-Welander disease: slowly progressive, uncommon adult forms, usual presentations, floppy baby, arthrogryposis, muscle weakness in infancy, diagnosis, weakness and wasting with areflexia, electrophysiology shows anterior horm cell disease, genetics, linked to chromosome 5q., neuronal apoptosis inhibitory protein (NAIP) gene, survival motor neuron (SMN) gene (12 Dec 1998) |
| infantile progressive 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) |
| 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) |
| juvenile spinal muscular atrophy | Slowly progressive proximal muscular weakness and wasting, beginning in childhood, caused by degeneration of motor neurons in the anterior horns of the spinal cord; onset usually between 2 and 17 years of age; usually autosomal recessive inheritance. Synonym: juvenile muscular atrophy, Kugelberg-Welander disease, Wohlfart-Kugelberg-Welander disease. (05 Mar 2000) |
| familial 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) |
| avoidant disorder of childhood | A mental disorder occurring in childhood or adolescence characterised by an excessive shrinking away from contact with people who are unfamiliar. Synonym: avoidant disorder of adolescence. (05 Mar 2000) |
| benign childhood epilepsy with centrotemporal spikes | A specific epilepsy syndrome beginning in childhood and remitting in adolescence, characterised by nocturnal simple partial motor seizures or generalised tonic-clonic seizures. EEG shows centrotemporal spikes that are activated by sleep and an otherwise normal EEG background. (05 Mar 2000) |
| papular acrodermatitis of childhood | <syndrome> A cutaneous manifestation of hepatitis B infection occurring in young children; an exanthem comprised of dusky papules on the legs, buttocks, and extensors of the arms; it lasts 2 to 8 weeks and is associated with adenopathy and malaise. Synonym: papular acrodermatitis of childhood. (05 Mar 2000) |
| recurrent pneumonia in childhood | <radiology> IMMUNE PROBLEMS, immune deficiency, chronic granulomatous disease of childhood, alpha-1 antitrypsin deficiency, ASPIRATION, GE reflux, H-type TE fistula, disorder of swallowing, oesophageal obstruction, UNDERLYING LUNG DISEASE, sequestration, brochopulmonary dysplasia, cystic fibrosis, atopic asthma, bronchiolitis obliterans, sinusitis, bronchiectasis, ciliary dysmotility syndromes, pulmonary foreign body (12 Dec 1998) |
| recurring digital fibromas of childhood | Multiple fibrous flesh-coloured nodules on the extensor aspect of the terminal phalanges of adjacent digits of infants and young children which often recur after attempted excision, do not metastasize, and may spontaneously regress in two to three years; composed of spindle cells containing cytoplasmic inclusions believed to be derived from myofibrils. Synonym: infantile digital fibromatosis. (05 Mar 2000) |
| mental disorders diagnosed in childhood | Those psychiatric disorders usually first diagnosed in infancy, childhood, or adolescence. These disorders can also be first diagnosed during other life stages. (12 Dec 1998) |
Synonyms : HMN (Hereditary Motor Neuropathy) Proximal Type I, Muscular Atrophy, Spinal, Type I, Muscular Atrophy, Spinal, Type II, Muscular Atrophy, Spinal, Type III, Proximal Hereditary Motor Neuropathy Type I, Spinal Muscular Atrophy Type I, Werdnig Hoffman Disease
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|