| 영문 | deafness | 한글 | 귀먹음, 난청 |
|---|---|---|---|
| 설명 | 청각이 저하 또는 상실된 상태. 원인과 정도는 여러 가지인데, 귀머거리는 그 정도가 가장 심한 상태이다. 청각의 전도경로에 장애가 있을 때 난청이 일어나고, 그 병터가 바깥귀길이나 가운데귀에 있는 것을 전음난청, 속귀에 있는 것을 감음난청이라 하여 구분한다. 또 병터의 자리를 명시하여 중이성 난청이나 미로성 난청 등으로 세분하기도 하며, 외상성 난청 등 원인별로 분류하기도 한다. 난청의 진단이나 예방-예후는 청력검사에 의하여 실시된다. |
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| GD | gastroduodenal; Gaucher disease; general diagnostics; general dispensary; gestational day; Gianotti ... |
|---|---|
| GDXY | XY gonadal dysgenesis |
| MGD | maximal glucose disposal; mixed gonadal dysgenesis |
| OASD | ocular albinism-sensorineural deafness [syndrome] |
| ADFN | albinism-deafness [syndrome]; albinism-deafness syndrome |
| GD | Gonadal dysgenesis |
|---|---|
| MGD | Mixed gonadal dysgenesis |
| SNHL | Sensorineural Hearing Loss |
| MIDD | Maternally Inherited Diabetes and Deafness |
| SD | Sudden deafness |
| sensorineural deafness | Hearing impairment due to disorders of the cochlear division of the 9th cranial nerve (auditory nerve), the cochlea, or the retrocochlear nerve tracts, as opposed to conductive deafness. (05 Mar 2000) |
|---|---|
| gonadal dysgenesis | <embryology, genetics> A rare genetic disorder in women that is characterised by the absence of an X chromosome. This disorder inhibits normal sexual development and causes infertility. Features include webbing of the neck, short stature, retarded development of secondary sex characteristics, absence of menses, coarctation of the aorta, low hairline, eye abnormalities (drooping eyelids) and skeletal deformities. Treatment include oestrogen supplementation at puberty. Growth hormone replacement may be necessary in some cases. Cardiac surgery may be necessary to correct coarctation of the aorta. Incidence: 1 in 3,000 births. (10 Oct 1997) |
| gonadal dysgenesis, 46,xy | A syndrome characterised by "streak gonads" in a phenotypic female with a 46,xy karyotype. It is due to a mutation which inhibits the function of the y-borne determinant that would normally cause the indifferent embryonic gonad to differentiate into a testis. The streak gonad is incapable of ovulation or oestrogen secretion. The syndrome is sometimes called "pure gonadal dysgenesis," but this designation may also refer to the presence of streak gonads with a 46,xx karyotype. (12 Dec 1998) |
| gonadal dysgenesis, mixed | A syndrome of gonadal dysgenesis in which there is a testis on one side and a "streak gonad" on the other. The phenotype is generally male, but may be female since the individual is a mosaic. Various karyotypes have been identified, including 45,xo/47,xyy; 45,xo/46,xy; and 45,xo/46,xyo. (12 Dec 1998) |
| hearing loss, sensorineural | Hearing loss resulting from damage to the sensory mechanism internal from the oval and round windows. (12 Dec 1998) |
| sensorineural hearing loss | <neurology> A form of deafness that occurs due to dysfunction of the auditory nerve (cranial nerve VIII). (27 Sep 1997) |
| seminiferous tubule dysgenesis | A disorder in which the seminiferous tubules exhibit an abnormal cytoarchitecture and extensive hyalinization; the testes are small, and few spermatozoa are formed; the body habitus may be eunuchoid, and gynaecomastia may be present; urinary gonadotropin output is usually high, and the incidence of mental deficiency and illness increased; sex chromatin may be male or female, and androgen secretion ranges from subnormal to normal. It is a constant feature of (and is often used synonymously with) Klinefelter's syndrome. Synonym: germinal aplasia. (05 Mar 2000) |
| hybrid dysgenesis | The inability of certain strains of the fruit fly Drosophila melanogaster to interbreed with each other because they produce offspring that are all sterile or offspring which have a high number of harmful mutations. (09 Oct 1997) |
| dysgenesis | Defective development. (18 Nov 1997) |
| iridocorneal mesodermal dysgenesis | Mesodermal dysgenesis of cornea and iris, producing pupillary anomalies, posterior embryotoxon, and secondary glaucoma. Synonym: Rieger's anomaly. (05 Mar 2000) |
| testicular dysgenesis | A congenital derangement of seminiferous tubular structure and function, resulting in male infertility; the defect in spermatogenesis may be incomplete, as in maturational arrest or premature sloughing, or spermatogenesis may be completely absent, as in the Sertoli-cell-only syndrome. (05 Mar 2000) |
| gonadal | <anatomy> Pertaining to a gonad. (18 Nov 1997) |
| gonadal agenesis | Congenital absence of essentially all gonadal tissue; the external genitalia and genital ducts are female, but if interstitial cells of Leydig are present, the external genitalia are commonly ambiguous and the genital ducts are female. See: gonadal dysgenesis. Compare: Klinefelter's syndrome, Turner's syndrome. Synonym: gonadal agenesis. (05 Mar 2000) |
| gonadal aplasia | Congenital absence of essentially all gonadal tissue; the external genitalia and genital ducts are female, but if interstitial cells of Leydig are present, the external genitalia are commonly ambiguous and the genital ducts are female. See: gonadal dysgenesis. Compare: Klinefelter's syndrome, Turner's syndrome. Synonym: gonadal agenesis. (05 Mar 2000) |
| gonadal cords | Columns of germinal and follicle cells penetrating centripetally into the embryonic ovarian or testicular cortex. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|