| 영문 | non-Hodgkin lymphoma | 한글 | 비호지킨 림프종 |
|---|---|---|---|
| 설명 | 림프종은 림프절에 생긴 악성 종양으로 백혈병과는 다르다. 백혈병은 골수에서 생긴 림프구성 악성종양이지만, 림프종은 림프조직에서 생긴 림프구성 악성종양이다. 크게 림프종은 2가지로 나눌 수 있는 데, 호지킨병(Hodgkin's lymphoma)과 비호지킨림프종(non-Hodgkin's lymphoma)으로 나눌 수 있다. 또한 비호지킨림프종은 여러 가지의 세포형태에 따라 나누고 있다. 이 병은 단지 림프절뿐만 아니라 지라, 골수, 이외 다른 기관을 침범함으로써 악성이며, 생명에 큰 위협을 준다. 악성림프종의 일종. 전이의 형태가 다양하여, 주위 림프절을 건너뛰어 다른 림프절로 전이하기도 한다. 또한 세포의 형태에 따라 여러 가지 종류가 있으며 대개 치료는 방사선치료와 화학요법을 복합하여 사용한다. |
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| 영문 | mosaicism | 한글 | 섞임증 |
|---|---|---|---|
| 설명 | 유전학에서 핵형 또는 유전자에서 볼 수 있는 현상으로 서로 다른 두 개 이상의 대립형질이 한개체내에 부분을 달리하여 존재하는 것. |
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| 영문 | trisomy | 한글 | 세염색체증 |
|---|---|---|---|
| 설명 | 이배수성 세포에 한 형의 제3염색체가 존재하는 것(2n+1). 즉, 상동염색체쌍 외에 한 개의 염색체를 여분으로 갖는 개체 또는 세포. 삼염색체라고도 한다. 여분으로 포함된 염색체가 상동염색체쌍 중 어느 한 염색체와 상동성이 있는 경우를 말한다. 상동성이 없을 때는 과잉염색체라고 한다. 추가되는 염색체는 상동염색체의 수만큼 가능하며, 1상동염색체가 세염색체로 되는 것 외에 복수의 염색체쌍이 세염색체로 되는 경우도 있다. 세염색체가 존재하면 감수분열에서는 특이한 3가염색체가 형성되고, 유전양식도 정상적인 2가염색체의 경우와 달리 3염색체성이 된다. 사람의 다운증후군은 제21의 세염색체에 원인이 있는 유전장애이다. |
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| ECG | Electro-Cardio-Graphy(-Gram); 심전도 = EKG 1. Conducting System Structu... |
|---|---|
| NANB | non-A, non-B [hepatitis] |
| NANBH | non-A, non-B hepatitis |
| non-REM | non-rapid eye movement [sleep] |
| G0 | quiescent phase of cells leaving the mitotic cycle |
| ND | non-disjunction |
|---|---|
| CPM | Confined placental mosaicism |
| Ts16 | Trisomy 16 |
| Ts19 | Trisomy 19 |
| T21 | Trisomy 21 |
| non-A, non-B, non-C hepatitis | Hepatitis caused by viral organisms other than hepatitis viruses A, B or C. (05 Mar 2000) |
|---|---|
| hepatitis non-A, non-B | <virology> A virus somewhat similar in size to Hepatitis A but has no antigenic cross reaction with either A or B. Many of the cases are in fact hepatitis C and this was the old term for hepatitis C. (20 Sep 2002) |
| non-A, non-B hepatitis | Hepatitis caused by two or more infectious agents not detectable by methods that reveal the presence of hepatitis viruses A and B; one cause, now called type C hepatitis has been identified; may follow blood transfusion and is often seen in chronic renal dialysis patients. Synonym: NANB hepatitis. (05 Mar 2000) |
| non-A, non-B hepatitis virus | Term used to group any of a number of viruses, other than A or B, which cause hepatitis in humans. (05 Mar 2000) |
| disjunction | The normal separation of pairs of chromosomes at the anaphase stage of meiosis I or II. Origin: dis-+ L. Junctio, a joining, fr. Jungo, pp. Junctum, to join (05 Mar 2000) |
| disjunction mutant | Drosophila mutant in which chromosomes are partitioned unequally between daughter cells at meiosis, as a result of nondisjunction. (18 Nov 1997) |
| gene mosaicism | <genetics> Descriptive of an organism that consists of two or more genetically distinct cell lines. (14 Nov 1997) |
| germinal mosaicism | Gonadal mosaicism, a state in which cells in a sector of a gonad are of a form not present in either parent, because of mutation in an intermediate progenitor of that sector. (05 Mar 2000) |
| cellular mosaicism | A chimerism in which a tissue contains cells from different zygotes; e.g., in humans, involving erythrocytes. (05 Mar 2000) |
| chromosome mosaicism | See: mosaic. (05 Mar 2000) |
| mosaicism | The occurrence in an individual of two or more cell populations of different chromosomal constitutions, derived from a single zygote. (12 Dec 1998) |
| syndrome, trisomy 13 | Condition with three rather than the normal two chromosomes 13. Children born with this syndrome have multiple malformations and mental retardation due to the extra chromosome 13. The congenital malformations (birth defects) commonly include scalp defects, more than haemangiomas more than (blood vessel malformations) of the face and nape of the neck, cleft lip more than and palate, malformations of the heart and abdominal organs, and flexed fingers with extra digits. The mental retardation is profound. The iq is untestably low. The majority of trisomy 13 babies die soon after birth or in infancy. The condition is also called patau syndrome after the late geneticist klaus patau more than (at the university of wisconsin) who discovered the extra chromosome in 1960. (12 Dec 1998) |
| syndrome, trisomy 18 | There are three instead of the normal two chromosomes 18. Children with this condition have multiple malformations and mental retardation due to the extra chromosome 18. The children characteristically have low birth weight, small head (microcephaly), small jaw (micrognathia), malformations of the heart and kidneys, clenched fists with abnormal finger positioning, and malformed feet. The mental retardation is profound with the iq too low to edven test. Nineteen out of 20 (95%) of these children die before their first birthday. The condition is also called edwards syndrome in honor of the british physician and geneticist john edwards who discovered the extra chromosome in 1960. (12 Dec 1998) |
| syndrome, trisomy 21 | A common chromosome disorder due to an extra chromosome number 21 (trisomy 21). The syndrome causes mental retardation, a characteristic face, and multiple malformations. It is associated with a major risk for heart problems, a lesser risk of duodenal atresia (part of the intestines not developed), and a minor but still significant risk of acute leukaemia. Trisome 21 syndr0ome is also commonly called down syndrome after the 19th century english doctor langdon down who was curiously enough not the first person to describe the condition, added little to knowledge and, in great error, attributed the condition to a reversion to the mongoloid race. The disorder was also once called mongolism, a term now considered slang. (12 Dec 1998) |
| trisomy | <genetics, molecular biology> Term which indicates the presence of an additional whole chromosome. Each cell usually has 46 but in trisomy this is increased to 47. (13 Nov 1997) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|