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Incontinentia pigmenti: A propósito de un caso / Incontinentia pigmenti
Rev. méd. hered ; 6(3): 140-4, sept. 1995. ilus
Article in Spanish | LILACS, LIPECS | ID: lil-176346
RESUMO
Incontinentia Pigmenti is a rare X-linked multisystem neuroectodermic disorder with signs and symptonms related mainly to the dermatologic, dental, ocular and central nervous systems, and characterized by death in the majority of male embryos. Affected children do not appear sick, in spite of the skin eruption, the peripheral leucocytosis and marked eosinophilia. Most of the cases are reported in caucasians, although there are description in black children, orientals, north, central and south american indians, and in our mestizos. The name of Incontinentia Pigmeti describes the incontinence of the melain pigment from the basal layer of the epidemermis into the superficial dermis
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Index: LILACS (Americas) Main subject: Incontinentia Pigmenti Limits: Child / Female / Humans / Infant, Newborn Language: Spanish Journal: Rev. méd. hered Year: 1995 Type: Article

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Index: LILACS (Americas) Main subject: Incontinentia Pigmenti Limits: Child / Female / Humans / Infant, Newborn Language: Spanish Journal: Rev. méd. hered Year: 1995 Type: Article