| 영문 | central nervous system(CNS) | 한글 | 중추신경계 |
|---|---|---|---|
| 설명 | 신경계는 중추신경계와 말초신경계로 분류할 수가 있다. 중추신경계란 뇌와 척수로 구성되어 있는 신경계를 이르는 말이다. 말초신경계란 이 이외의 모든 신경계를 이르는 말이다. |
||
| 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. |
||
| 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. |
||
| AFP | Alpha(α) Feto-Protein [HP 1826, 1858, 1859, 2265] ; Oncofetal Antigens &nbs... |
|---|---|
| CHARGE Associations | Coloboma Heart disease Atresia choanae Reta... |
| CNS | Central Nervous System; 중추신경계 |
| CHARGE | coloboma, heart disease, atresia choanae, retarded growth and retarded development and/or CNS anomal... |
| CNS | central nervous system; clinical nurse specialist; coagulase-negative staphylococci; congenital neph... |
| CNS | Canadian Neurological Scale |
|---|---|
| CNS | cental nervous system |
| CNS | Clinical Nurse Specialist |
| CNS | Coagulase Negative Staphylococci |
| CNS | Coagulase Negative Staphylococcus |
| CNS | <anatomy, neurology> Pertaining to the brain, cranial nerves and spinal cord. It does not include muscles or peripheral nerves. In invertebrates, the central nervous system is composed of the segmental ganglia of the ventral nerve cord together with the fused ganglia or brain at the anterior end. Acronym: CNS (12 Jan 1998) |
|---|---|
| CNS leukaemia | <oncology> Invasion of the brain or spinal cord by leukaemic cells. This may be diagnosed by examination of the surrounding cerebrospinal fluid. Origin: Gr. Haima = blood (13 Nov 1997) |
| CNS lipoma | <radiology> Incidence: less than1% of brain tumours, age: presentation in childhood/adulthood, associated with agenesis of corpus callosum in 50%, assymptomatic in 50% location: genu of corpus callosum (25-50%), tuber cinerum, quadrigeminal region, chiasmatic, interpeduncular, sylvian, CP angle, and cerebellomedullary cisterns findings: -100 HU on CT, occasionally calcified rim (especially in corpus callosum), no enhancement, hyperintense on T1 (characteristic) (12 Dec 1998) |
| CNS prophylaxis | Chemotherapy or radiation therapy to the central nervous system (CNS). This is preventative treatment. It is given to kill cancer cells that may be in the brain and spinal cord, even though no cancer has been detected there. (12 Dec 1998) |
| 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) |
| childhood | The period of life between infancy and puberty. (05 Mar 2000) |
| childhood absence epilepsy | A generalised epilepsy syndrome characterised by the onset of absence seizures in childhood, typically at age six or seven years. There is a strong genetic predisposition and girls are affected more often than boys. EEG reveals generalised 3 Hz spike-wave activity on a normal background. Prognosis for remission is good if the patient does not also have generalised tonic-clonic seizures. See: absence. Synonym: petit mal epilepsy, pyknolepsy. (05 Mar 2000) |
| childhood epilepsy with occipital paroxysms | A benign epilepsy syndrome characterised by frequent occipital spikes often activated by eye closure. It has a seizure semiology that includes visual manifestations; not always remitting later in life. (05 Mar 2000) |
| 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) |
| childhood schizophrenia | A severe emotional disturbance of childhood characterised by qualitative impairment in reciprocal social interaction and in communication, language, and social development. Synonym: autistic disorder, childhood schizophrenia, early infantile autism, Kanner's syndrome. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|