| 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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| 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 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) |
| 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) |
| stratum pigmenti bulbi | The outer layer of the retina, consisting of pigmented epithelium. Synonym: ectoretina, stratum pigmenti bulbi, stratum pigmenti retinae, tapetum nigrum, tapetum oculi. (05 Mar 2000) |
| stratum pigmenti corporis ciliaris | The continuation of the pigment layer of the retina onto the posterior aspect of the ciliary body. Synonym: pigmented layer of ciliary body. (05 Mar 2000) |
| stratum pigmenti iridis | The double layer of pigmented epithelium on the posterior surface of the iris. Synonym: pigmented layer of iris. (05 Mar 2000) |
| stratum pigmenti retinae | The outer layer of the retina, consisting of pigmented epithelium. Synonym: ectoretina, stratum pigmenti bulbi, stratum pigmenti retinae, tapetum nigrum, tapetum oculi. (05 Mar 2000) |
Synonyms : Bloch Sulzberger Syndrome, Syndrome, Bloch-Sulzberger
| incontinentia pigmenti |
Incontinentia pigmenti (IP) is a disorder that affects the skin, hair, teeth, and nails. The skin lesions evolve through characteristic stages: 1) blistering (from birth to about four months of age), 2) a wart-like rash (for several months), 3) swirling macular hyperpigmentation (from about six months of age into adulthood), followed by 4) linear hypopigmentation. Alopecia, hypodontia, abnormal tooth shape, and dystrophic nails are observed. ...
Ãâó: en.wikipedia.org/wiki/Incontinentia_pigmenti
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