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incontinentia pigmenti/edema
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Hydrops fetalis in three male fetuses of a female with incontinentia pigmenti.
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OBJECTIVE
Careful investigation of hydrops fetalis (HF) is important with regard to genetic counselling and prenatal diagnosis. HF is known to be associated with various genetic disorders. To date there has been only one report of a male fetus in whom incontinentia pigmenti (IP) was associated with
Incontinentia pigmenti (Bloch-Sulzberger syndrome) in neonates.
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A female newborn presented with emerging skin lesions, systemic eosinophilia, and eosinophilic reaction in the skin, liver, lungs, spleen, lymphatic nodes, porencephalia, convulsions, and disorders of thermoregulation. In addition to that, respiratory and heart failure, as well as brain edema were
Computed tomographic demonstration of brain changes in incontinentia pigmenti.
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Incontinentia pigmenti is a rare condition, which may involve the central nervous system. Computed tomographic (CT) examination can supply important information about the dynamics and pathologic nature of this poorly understood syndrome. Two patients suffering from incontinentia pigmenti were
Retinal and other manifestations of incontinentia pigmenti (Bloch-Sulzberger syndrome).
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BACKGROUND
One of the largest series of patients with incontinentia pigmenti who have undergone detailed ophthalmologic examination is reported here, including previously unrecognized findings with visually disabling consequences.
METHODS
Thirteen females with incontinentia pigmenti from eight
Ultrastructural findings in incontinentia pigmenti.
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From their ultrastructural study of incontinenti pigmenti, the authors confirm that in this condition there is no pigmentary anomaly, but that pigmentation is the last step of a still unknown process. At birth those who are affected display an intracellular edema which leads to the formation of a
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