| MRF | Markov random field; medical record file; melanocyte-[stimulating hormone]-releasing factor; mesence... |
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| ASMD | anterior segment mesenchymal dysgenesis; atonic sclerotic muscle dystrophy |
| ASOD | anterior segmental ocular dysgenesis |
| FDTS | familial testicular dysgenesis syndrome |
| GD | gastroduodenal; Gaucher disease; general diagnostics; general dispensary; gestational day; Gianotti ... |
| GD | Gonadal dysgenesis |
|---|---|
| MGD | Mixed gonadal dysgenesis |
| mdg | Muscular dysgenesis |
| RTD | Renal tubular dysgenesis |
| MRF | Mesencephalic Reticular Formation |
| 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) |
| 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) |
| reticular | <anatomy> Pertaining to or resembling a net. (16 Dec 1997) |
| reticular activating system | <physiology> A physiological term denoting that part of the brainstem reticular formation that plays a central role in the organism's bodily and behavorial alertness. It extends as a diffusely organised neural apparatus through the central region of the brainstem into the subthalamus and the intralaminar nuclei of the thalamus; by its ascending connections it affects the function of the cerebral cortex in the sense of behavioural responsiveness; its descending (reticulospinal) connections transmit its activating influence upon bodily posture and reflex mechanisms (e.g., muscle tonus), in part by way of the gamma motor neurons. See: reticular formation. Synonym: non-specific system. (05 Mar 2000) |
| reticular cartilage | <anatomy> Rarely used terms for fibrocartilage. (05 Mar 2000) |
| reticular cell | A cell with processes making contact with those of other similar cell's to form a cellular network; along with the network of reticular fibres, the reticular cell's form the stroma of bone marrow and lymphatic tissues. (05 Mar 2000) |
| reticular degeneration | <ophthalmology> Severe epidermal oedema resulting in multilocular bullae. (05 Mar 2000) |
| reticular dystrophy of cornea | <ophthalmology> Bilateral, progressive, superficial degeneration of the corneal epithelium and adjacent Bowman's membrane. (05 Mar 2000) |
| reticular erythematous mucinosis | <syndrome> A reticular erythematous dermatitis of the upper trunk, more common in women, in which there is perivascular infiltrate of lymphocytes, few plasma cells, and upper dermal deposits of mucin; worsens on exposure to ultraviolet light. Synonym: reticular erythematous mucinosis. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|