| 영문 | sign | 한글 | 징후 |
|---|---|---|---|
| 설명 | 겉으로 나타나는 낌새. 즉, 어떤 병의 존재를 표시하는 병의 객관적 소견 또는 증거. 이에 대하여 환자가 질환에 의해 자각적으로 불편감을 느끼는 증상(symptom)은 환자의 주관적 감각으로 구별된다. |
||
| 영문 | vital sign | 한글 | 활력징후 |
|---|---|---|---|
| 설명 | 인간이 살아있는 징후, 즉 생명징후를 말한다. 호흡, 맥박, 체온, 의식정도, 혈압을 지표로 한다. 구급의료의 현장에서 환자의 상태를 파악하는데 유용하다. |
||
| R-C sign(spot) | Red Cherry sign(spot) |
|---|---|
| HC | hair cell; hairy cell; handicapped; head circumference; head compression; health care; healthy contr... |
| HD | Haab-Dimmer [syndrome]; Hajna-Damon [broth]; Hansen disease; hearing distance; heart disease; helix ... |
| HDA | heteroduplex analysis; Huntington Disease Association; hydroxydopamine |
| CFVS | cerebrospinal fluid flow void sign |
| A.S.L. | American Sign Language |
|---|---|
| HC | Huntington chorea |
| UHDRS | Unified Huntington Disease Rating Scale |
| Huntington | George, U.S. Physician, 1850-1916. See: Huntington's chorea, Huntington's disease. (05 Mar 2000) |
|---|---|
| Huntington chorea | <neurology> An inherited adult-onset disease of the central nervous system. It is characterised by dementia and bizarre involuntary movements. The disease is progressive and there is currently no known cure. The identification of the gene (huntingtin) on chromosome 4p now allows for direct mutation analysis. The gene contains a trinucleotide repeat (CAG) that is found to be expanded in length in affected patients. The normal allele size ranges from 11 to 34 triplet repeat units, while 42 repeats or greater is considered diagnostic of Huntington disease. As in other trinucleotide repeat disorders, the phenomenom of anticipation has been observed, in this case expressed as earlier age of onset in offspring, particularly with paternal transmission. A further complication is the presence of two neighboring trinucleotide repeats (both CCG) which can expand independently without causing the disease. Early PCR primer sets encompassed these adjacent repeats, potentially yielding false positive test results, newer primers hone in more closely on the CAG repeat sequence. Careful attention must be paid to the psychosocial support structure of prospective test subjects in Huntington disease genetic counseling. Established protocols require systematic neuropsychiatric assessment and informed consent prior to DNA testing. Inheritance: autosomal dominant. (29 Dec 1997) |
| Huntington disease | <neurology> An inherited adult-onset disease of the central nervous system. It is characterised by dementia and bizarre involuntary movements. The disease is progressive and there is currently no known cure. The identification of the gene (huntingtin) on chromosome 4p now allows for direct mutation analysis. The gene contains a trinucleotide repeat (CAG) that is found to be expanded in length in affected patients. The normal allele size ranges from 11 to 34 triplet repeat units, while 42 repeats or greater is considered diagnostic of Huntington disease. As in other trinucleotide repeat disorders, the phenomenom of anticipation has been observed, in this case expressed as earlier age of onset in offspring, particularly with paternal transmission. A further complication is the presence of two neighboring trinucleotide repeats (both CCG) which can expand independently without causing the disease. Early PCR primer sets encompassed these adjacent repeats, potentially yielding false positive test results, newer primers hone in more closely on the CAG repeat sequence. Careful attention must be paid to the psychosocial support structure of prospective test subjects in Huntington disease genetic counseling. Established protocols require systematic neuropsychiatric assessment and informed consent prior to DNA testing. Inheritance: autosomal dominant. (29 Dec 1997) |
| Huntington's chorea | A progressive disorder usually beginning in young to middle age, consisting of a triad of choreoathetosis, dementia, and autosomal dominant inheritance with complete penetrance. Bilateral marked wasting of the putamen and the head of the caudate nucleus is characteristic. Synonym: chronic progressive chorea, degenerative chorea, hereditary chorea, Huntington's disease. (05 Mar 2000) |
| huntington's disease | An hereditary disorder with mental and physical deterioration leading to death. Although characterised as an adult-onset disease (as is usually the case), we have seen children with full-blown huntington's disease. (12 Dec 1998) |
| disease, huntington's | An hereditary disorder with mental and physical deterioration leading to death. Although characterised as an adult-onset disease (as is usually the case), we have seen children with full-blown Huntington's disease. (12 Dec 1998) |
| Aaron's sign | <clinical sign> In acute appendicitis, a referred pain or feeling of distress in the epigastrium or precordial region on continuous firm pressure over McBurney's point. (05 Mar 2000) |
| Abadie's sign of tabes dorsalis | Insensibility to pressure over the tendo achillis. (05 Mar 2000) |
| Abrahams' sign | <clinical sign> An obsolete sign: Rales and other adventitious sounds, changes in the respiratory murmurs, and increase in the whispered sound can be heard on auscultation over the acromial end of the clavicle some time before they become audible at the apex; heard primarily in pulmonary tuberculosis affecting the apical portion of the lung, a dull-flat note, i.e., one between the normal dullness at the right apex and absolute flatness, heard on percussion in that region, indicating progress from incipient to advanced tuberculosis. (05 Mar 2000) |
| accessory sign | <clinical sign> A finding frequently but not consistently present in a disease. Synonym: assident sign. (05 Mar 2000) |
| Allis' sign | <clinical sign> In fracture of the neck of the femur, the trochanter rides up, relaxing the fascia lata, so that the finger can be sunk deeply between the great trochanter and the iliac crest. (05 Mar 2000) |
| Amoss' sign | <clinical sign> In painful flexion of the spine, it is necessary to support a sitting position by extending the arms behind the torso with the weight placed on the hands. (05 Mar 2000) |
| Anghelescu's sign | <clinical sign> In vertebral tuberculosis, painful or impossible flexion of the spine when the patient attempts to rest weight on the heels and occiput. (05 Mar 2000) |
| antecedent sign | <clinical sign> A sign that appears during the prodrome of a disease. Synonym: antecedent sign. (05 Mar 2000) |
| assident sign | <clinical sign> A finding frequently but not consistently present in a disease. Synonym: assident sign. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|