Incontinentia Pigmenti

Scientific BACKGROUND: Incontinensia pigmenti is an X-linked genetic disorder characterised by the involvement of skin, hair, teeth and central nervous system (CNS). Skin lesions secondary to melanin is typical. Depending on the CNS involvement, cognitive disturbances, mental retardation, muscle wea...

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Main Authors: Cengiz Yalçınkaya, Gülçin Benbir
Format: Article
Language:English
Published: Galenos Yayinevi 2007-10-01
Series:Türk Nöroloji Dergisi
Subjects:
Online Access:http://www.tjn.org.tr/jvi.aspx?pdir=tjn&plng=eng&un=TJN-97269
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author Cengiz Yalçınkaya
Gülçin Benbir
author_facet Cengiz Yalçınkaya
Gülçin Benbir
author_sort Cengiz Yalçınkaya
collection DOAJ
description Scientific BACKGROUND: Incontinensia pigmenti is an X-linked genetic disorder characterised by the involvement of skin, hair, teeth and central nervous system (CNS). Skin lesions secondary to melanin is typical. Depending on the CNS involvement, cognitive disturbances, mental retardation, muscle weakness and seizures may occur. CASE: Seven-year-old girl had partial seizures at 5-days of age. During newborn period, she had vesicular lesions with relative pigmented edges and prone to form plaques all over her extremities, the biopsy from which revealed the diagnosis of incontinensia pigmenti. Seizures responded well to medical treatment repeated at the end of 6 years of drug-free period. EEG showed right frontal neuronal hyperexitability, and cranial MRI demonstrated atrophy in the right hemisphere. At the last examination, skin lesions were prominently diminished, leaving small, hyperpigmented scars limited to some parts of the body only. CONCLUSION: This case report emphasizes that in patients who admit with seizures, examination of skin and careful questioning of previous skin lesions are of diagnostic importance
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spelling doaj.art-f4375d023ef44871aa4d56ea591b33432023-02-15T16:19:23ZengGalenos YayineviTürk Nöroloji Dergisi1301-062X1309-25452007-10-01135351357Incontinentia PigmentiCengiz Yalçınkaya0Gülçin Benbir1Department Of Neurology, İstanbul University, Cerrahpasa Faculty Of Medicine, İstanbul, TurkeyDivision Of Neurology, Department Of Pediatrics, İstanbul University, Cerrahpasa Faculty Of Medicine, İstanbul, TurkeyScientific BACKGROUND: Incontinensia pigmenti is an X-linked genetic disorder characterised by the involvement of skin, hair, teeth and central nervous system (CNS). Skin lesions secondary to melanin is typical. Depending on the CNS involvement, cognitive disturbances, mental retardation, muscle weakness and seizures may occur. CASE: Seven-year-old girl had partial seizures at 5-days of age. During newborn period, she had vesicular lesions with relative pigmented edges and prone to form plaques all over her extremities, the biopsy from which revealed the diagnosis of incontinensia pigmenti. Seizures responded well to medical treatment repeated at the end of 6 years of drug-free period. EEG showed right frontal neuronal hyperexitability, and cranial MRI demonstrated atrophy in the right hemisphere. At the last examination, skin lesions were prominently diminished, leaving small, hyperpigmented scars limited to some parts of the body only. CONCLUSION: This case report emphasizes that in patients who admit with seizures, examination of skin and careful questioning of previous skin lesions are of diagnostic importancehttp://www.tjn.org.tr/jvi.aspx?pdir=tjn&plng=eng&un=TJN-97269Incontinensia pigmentiepilepsycerebral hemiatrophy
spellingShingle Cengiz Yalçınkaya
Gülçin Benbir
Incontinentia Pigmenti
Türk Nöroloji Dergisi
Incontinensia pigmenti
epilepsy
cerebral hemiatrophy
title Incontinentia Pigmenti
title_full Incontinentia Pigmenti
title_fullStr Incontinentia Pigmenti
title_full_unstemmed Incontinentia Pigmenti
title_short Incontinentia Pigmenti
title_sort incontinentia pigmenti
topic Incontinensia pigmenti
epilepsy
cerebral hemiatrophy
url http://www.tjn.org.tr/jvi.aspx?pdir=tjn&plng=eng&un=TJN-97269
work_keys_str_mv AT cengizyalcınkaya incontinentiapigmenti
AT gulcinbenbir incontinentiapigmenti