| 영문 | deciduous tooth | 한글 | 젖니, 탈락치아 |
|---|---|---|---|
| 설명 | 생후 7~8개월부터 약 2년반 동안에 나와 7~12세에 차례로 빠져서 새로운 치아로 교환되는 치아로, 20개가 존재한다. 색조는 백색 또는 청백색을 띠고 있다. 치관 길이는 짧지만, 근원 심경은 비교적 크며, 맞붙어 있는 치아면 접촉으로 인해 치경부 협착이 현저하다. 제일 유구치의 뺨쪽에는 치경부 부근에 띠 모양의 팽대부(치대)가 있다. 유구치근의 근분기부 바로 아래는 후속 영구치의 치배가 있기 때문에, 치근은 열려 있다. 치근은 연령에 따라 점차 흡수되어 간다. 치수강은 수실이 넓다. |
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| 영문 | wisdom Tooth | 한글 | 지치, 사랑니 |
|---|---|---|---|
| 설명 | 동양에서는 이 이빨이 날 때가 되면 사랑에 빠진다 하여 사랑니라 하지만, 서양에서는 지혜가 생긴다 하여 지치(지혜니)라고 한다. 가장 늦게 발생하는 어금니로써 가장 안쪽에 있으며, 없는 경우도 있다. 대개 그 자라나는 방향이 위이빨에서는 다른 이빨에 큰 지장이 없으나, 아래쪽에 있는 이빨에서는 다른 어금니의 뿌리를 건드리는 쪽으로 나는 경우가 많으므로, 꼭 빼낼 것을 권장하기도 한다. |
||
| ECG | Electro-Cardio-Graphy(-Gram); 심전도 = EKG 1. Conducting System Structu... |
|---|---|
| CMT | California mastitis test; cancer multistep therapy; catechol methyltransferase; certified medical tr... |
| CMTD | Charcot-Marie-Tooth disease |
| CMTS | Charcot-Marie-Tooth syndrome |
| CMTX | Charcot-Marie-Tooth [syndrome], X-linked |
| BBTD | Baby Bottle Tooth Decay |
|---|---|
| CMT | Charcot Marie Tooth |
| CMT | Charcot--Marie--Tooth disease |
| CMT1 | Charcot--Marie--Tooth disease type 1 |
| CMT1A | Charcot-Marie Tooth disease type 1A |
tooth brush
| 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) |
| infantile autism | 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) |
| infantile beriberi | Beriberi appearing in a breast-fed infants whose mother has beriberi due to thiamin deficiency. It is mainly the "wet" form of beriberi, characterised by heart failure with marked peripheral oedema (which is otherwise unusual in heart failure in infancy). An often fatal disease, acute in onset, which was formerly common in the Far Eastern countries where rice is consumed; reversible with thiamin. (05 Mar 2000) |
| infantile brain tumours | <radiology> Can be present at birth: choroid plexus papilloma, medulloblastoma, craniopharyngioma, ependymoma, astrocytoma, teratoma (12 Dec 1998) |
| infantile cataract | A cataract affecting a very young child. (05 Mar 2000) |
| infantile coeliac disease | Gluten-sensitive enteropathy appearing in infancy, often before the age of 9 months and characterised by acute onset, diarrhoea, abdominal pain, and "failure to thrive." (05 Mar 2000) |
| infantile colic | Episodes of abdominal pain due to abnormal muscular contraction of the intestine in infants. (05 Mar 2000) |
| infantile convulsion | Any convulsion occurring in infancy (0 to 2 years of age). (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|