| IP | icterus praecox; imaging plate; immune precipitate; immunoblastic plasma; immunoperoxidase technique... |
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| IPA | immunoperoxidase assay; incontinentia pigmenti achromians; independent physician or practice associa... |
| IP | Incontinentia Pigmenti |
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| syndrome, incontinentia pigmenti | A genetic disease with blisters that develop soon after birth on the trunk and limbs, then heal, but leave dark (hyperpigmented) streaks and marble-like whorls on the skin. (the name came from the erroneous idea that the skin cells were incontinent of pigment and could not contain it normally.) other key features of ip include dental and nail abnormalities, bald patches, and (in about 1/3rd of cases) mental retardation. Ip is an x-linked dominant with male lethality. The ip gene is in band q28 on the x chromosome. Mothers with ip have an equal chance of having a normal or ip daughter or a normal son. The ip sons die before birth. Ip is also known as bloch-sulzberger syndrome. (12 Dec 1998) |
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| incontinentia | <gastroenterology, urology> The inability to control excretory functions, as defecation (faecal incontinence) or urination (urinary incontinence). Origin: L. Incontinentia (13 Nov 1997) |
| incontinentia pigmenti | A genetic disease with blisters that develop soon after birth on the trunk and limbs, then heal, but leave dark (hyperpigmented) streaks and marble-like whorls on the skin. (the name came from the erroneous idea that the skin cells were incontinent of pigment and could not contain it normally.) other key features of ip include dental and nail abnormalities, bald patches, and (in about 1/3rd of cases) mental retardation. Ip is an x-linked dominant with male lethality. The ip gene is in band q28 on the x chromosome. Mothers with ip have an equal chance of having a normal or ip daughter or a normal son. The ip sons die before birth. Ip is also known as bloch-sulzberger syndrome. (12 Dec 1998) |
| incontinentia pigmenti achromians | Inherited hypopigmented macules in a "marble-cake" pattern, variably associated with epidermal nevi, alopecia, and ocular, skeletal, and neural abnormalities. Synonym: hypomelanosis of Ito. (05 Mar 2000) |
| velamen vulvae | Hypertrophy of the labia minora. (05 Mar 2000) |
| rima vulvae | The cleft between the labia majora. Synonym: rima pudendi, fissura pudendi, pudendal cleavage, pudendal slit, rima vulvae, urogenital cleft, vulvar slit. (05 Mar 2000) |
| pruritus vulvae | Intense itching of the external female genitals. (12 Dec 1998) |
| elephantiasis vulvae | Swelling of the vulval tissues due to lymphatic obstruction; in some cases it may be caused by filariasis, with induration or ulceration of the skin. Synonym: elephantiasis vulvae. (05 Mar 2000) |
| ulcus vulvae acutum | A simple acute ulceration of the vulva or lower vagina of nonvenereal origin. Synonym: ulcus vulvae acutum. (05 Mar 2000) |
| kraurosis vulvae | An atrophic disease affecting the female external genitalia, most often of older women, resulting in drying and shriveling of the parts, and marked by leukoplakic patches on the mucosa, itching, dyspareunia, dysuria, and soreness. It occurs most commonly as a result of lichen sclerosus et atrophicus of the vulva, but may be associated with other types of genital atrophy. (12 Dec 1998) |
| leukoplakia vulvae | A clinical term for hyperkeratotic white patches of the vulvar epithelium; biopsy is necessary for specific diagnosis. Synonym: leukoplakic vulvitis. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|