| Sulzberger, Marion | <person> U.S. Dermatologist, 1895-1983. See: Bloch-Sulzberger disease, syndrome, Sulzberger-Garbe disease, Sulzberger-Garbe syndrome. (05 Mar 2000) |
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| Marion, Georges | <person> French urologist, 1869-1932. See: Marion's disease. (05 Mar 2000) |
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| Marion's disease | A congenital obstruction of the posterior urethra. (05 Mar 2000) |
| Sims, J Marion | <person> U.S. Gynecologist, 1813-1883. See: Sims' position, Sims uterine sound. (05 Mar 2000) |
| Dorset, Marion | <person> U.S. Bacteriologist, 1872-1935. See: Dorset's culture egg medium. (05 Mar 2000) |
| Bloch-Sulzberger disease | 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) |
| Bloch-Sulzberger syndrome | 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) |
| Sulzberger-Garbe disease | Disease resembling an exudative form of nummular eczema described in Jewish males with oval lesions on the penis, trunk, and face. Synonym: exudative discoid and lichenoid dermatitis, Sulzberger-Garbe syndrome. (05 Mar 2000) |
| Sulzberger-Garbe syndrome | Disease resembling an exudative form of nummular eczema described in Jewish males with oval lesions on the penis, trunk, and face. Synonym: exudative discoid and lichenoid dermatitis, Sulzberger-Garbe syndrome. (05 Mar 2000) |
| syndrome, bloch-sulzberger | Also known as incontinentia pigmenti (ip). 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) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|