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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1-2
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pubmed:dateCreated |
1989-10-11
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pubmed:abstractText |
The case of a 7-year-old girl, born from a monochorionic biamniotic pregnancy (with healthy male twin) is presented. The patient showed a congenital brown-yellowish, raised, rough and oval-shaped nevic neoformation of the right temporo-zygomatic region. At 28 days of age she had a right hemiclonic status epilepticus, and from the 8th month of life she presented right sided partial motor seizures. Moreover from the beginning, her development milestones were delayed. When she was 5 years old an electroencephalogram displayed a sharp asymmetrical background activity, a continuous paroxysmal activity on the right hemisphere and independent focal irritative anomalies on the left posterior region. Her computed tomographic scan demonstrated megalencephaly on the right hemisphere. A biopsy specimen of her skin lesion showed the histological characteristics of a nevus sebaceous of Jadassohn. Taken together the clinical, neuroradiological and dermatological data led to the diagnosis of linear nevus sebaceous syndrome.
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pubmed:language |
ita
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:issn |
0026-4741
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
124
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
55-8
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:2767720-Cerebral Cortex,
pubmed-meshheading:2767720-Child,
pubmed-meshheading:2767720-Diseases in Twins,
pubmed-meshheading:2767720-Facial Neoplasms,
pubmed-meshheading:2767720-Female,
pubmed-meshheading:2767720-Humans,
pubmed-meshheading:2767720-Intellectual Disability,
pubmed-meshheading:2767720-Male,
pubmed-meshheading:2767720-Nevus, Pigmented,
pubmed-meshheading:2767720-Sebaceous Gland Neoplasms,
pubmed-meshheading:2767720-Syndrome,
pubmed-meshheading:2767720-Twins, Dizygotic
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pubmed:articleTitle |
[Sebaceous linear nevus syndrome with hemimegalencephaly. Report of a case].
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pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|