Results 171 to 180 of about 3,858 (212)
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Incontinentia Pigmenti in Nigerians
International Journal of Dermatology, 1983ABSTRACT:Three cases of incontinentia pigmenti were seen among Nigerian children who had had previously unreported occurrences of non‐development of Broca's speech area, signs suggestive of heterozygote albinism.
Y, Olumide, M, Danesi, T, McMoli
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Basophils in incontinentia pigmenti
Journal of the American Academy of Dermatology, 1984Incontinentia pigmenti is a rare genodermatosis of unknown etiology. A female infant with features typical of this disease was found to have basophils in early vesicular lesions. Mediators from these cells may be responsible for the accumulation of eosinophils in these lesions.
F C, Schmalstieg +3 more
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On the Inheritance of Incontinentia Pigmenti
Dermatologica, 2009A family in which the mother and 2 of her daughters were affected with incontinentia pigmenti is reported. To prove the genetic transmission of the disease on the basis that it is due to a single dominant gene on the X-chromosome with lethal effect in the hemizygous male, the authors studied 3 X-linked genetic markers (Xg blood group, glucose-6 ...
J M, Cantu-Garza, E, Ruiz-Barquin
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American Journal of Diseases of Children, 1985
We describe 15 patients with incontinentia pigmenti whom we have followed up from two to 11 years. This longitudinal approach allowed us to observe the course of the skin lesions and developmental progress of these children. We found that in contrast to what has been previously reported in most of the literature, the bullous and verrucous lesions do ...
J E, O'Brien, M, Feingold
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We describe 15 patients with incontinentia pigmenti whom we have followed up from two to 11 years. This longitudinal approach allowed us to observe the course of the skin lesions and developmental progress of these children. We found that in contrast to what has been previously reported in most of the literature, the bullous and verrucous lesions do ...
J E, O'Brien, M, Feingold
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A.M.A. Archives of Dermatology, 1958
Incontinentia pigmenti usually begins in early childhood as a series of linear and grouped vesicles on an erythematous base, which, when ruptured, tend to become impetiginized. These may disappear and recur for weeks or months, gradually giving way to an intermediate temporary stage of linear verrucous lesions, or the vesicles may lead directly to the ...
S D, MARTY, H B, BECHTEL, C E, WOOD
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Incontinentia pigmenti usually begins in early childhood as a series of linear and grouped vesicles on an erythematous base, which, when ruptured, tend to become impetiginized. These may disappear and recur for weeks or months, gradually giving way to an intermediate temporary stage of linear verrucous lesions, or the vesicles may lead directly to the ...
S D, MARTY, H B, BECHTEL, C E, WOOD
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Incontinentia Pigmenti Coxsackium
Pediatric Dermatology, 2016AbstractLate recurrences of first‐stage inflammatory vesiculobullous lesions of incontinentia pigmenti (IP) are uncommon but have been reported to occur in the setting of infections, fevers, and vaccinations. This phenomenon has not been described in the setting of atypical hand, foot, and mouth disease (HFMD).
Julie, Jefferson, Anna, Grossberg
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Incontinentia pigmenti in adults
American Journal of Medical Genetics Part A, 2019AbstractIncontinentia Pigmenti (IP; MIM 308300) is an X‐linked dominant genodermatosis caused by pathogenic variant in IKBKG. The phenotype in adults is poorly described compared to that in children. Questionnaire survey of 99 affected women showed an age at diagnosis from newborn to 41 years, with 53 diagnosed by 6 months of age and 30 as adults ...
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Neonatal incontinentia pigmenti
Italian Journal of Dermatology and Venereology, 2023Astrid, Herzum +4 more
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THE GENETICS OF INCONTINENTIA PIGMENTI.
Archives of dermatology, 1996The familial incidence of incontinentia pigmenti and its almost exclusive occurrence in females have been explained by two theories. One theory (Pfeiffer) suggests that the disease is due to an autosomal, dominant gene, which is sex-limited in its expression, producing the defect only in females.
H O, Curth, D, Warburton
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