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neurocutaneous syndromes/palavik

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ArtiklidKliinilistes uuringutesPatendid
10 tulemused

Evaluation of the child who convulses with fever.

Ainult registreeritud kasutajad saavad artikleid tõlkida
Logi sisse
Febrile seizures result from age-dependent hyperexcitability of the brain that is induced by fever. Although there are important genetic influences that render a febrile child more likely to develop seizures, it is the fever per se that causes the seizure. Of primary importance in the diagnostic

Gómez-López-Hernández syndrome in a Japanese patient: a case report.

Ainult registreeritud kasutajad saavad artikleid tõlkida
Logi sisse
Gómez-López-Hernández syndrome (GLHS) is a rare neurocutaneous syndrome characterized by the triad of rhombencephalosynapsis, trigeminal anesthesia, and bilateral parieto-occipital alopecia. We herein describe the first Japanese patient with GLHS characterized by the standard triad with typical
Tuberous sclerosis complex (TSC) is a relatively rare, autosomal dominant, and progressive neurocutaneous disorder involving multiple organs. Heterozygous mutations in the TSC1 gene located on chromosome 9 (9q34.13) or the TSC2 gene located on chromosome 16 (16p13.3) have been shown to

[Neurologic diseases and chromosome 17].

Ainult registreeritud kasutajad saavad artikleid tõlkida
Logi sisse
On the short arm of the 17th chromosome is a peripheral myelin protein (PMP22) the duplication or point mutation of which causes the development of some congenital autosomal dominant hereditary demyelinization neuropathies: the most frequent variants of Charcot-Marie-Tooth disease (CMT1A), some

Zoster vaccine live.

Ainult registreeritud kasutajad saavad artikleid tõlkida
Logi sisse
Herpes zoster is a neurocutaneous disease caused by the varicella-zoster virus and is associated with significant morbidity and long-term sequelae in older adults. Until recently, treatment options for these complications have been primarily targeted at disease state management and symptom relief.

[Imaging in paediatric epilepsy].

Ainult registreeritud kasutajad saavad artikleid tõlkida
Logi sisse
Epilepsy is a chronic disease, often with an onset during childhood and characterized by spontaneous and recurrent seizures. It concerns 0.5-1% of children under 16 years of age. A classification proposed by the International League Against Epilepsy (ILEA) in 2001 takes into account recent genetic

Progressively intractable seizures, focal alopecia, and hemimegalencephaly.

Ainult registreeritud kasutajad saavad artikleid tõlkida
Logi sisse
We report a 3-year-old boy with the neurocutaneous combination of unilateral alopecia, ipsilateral hemimegalencephaly, and intractable seizures. He was born with an asymmetric hair pattern consisting of absent patches of hair, a small left eyebrow, and less eyelashes on the left eye; he had normal
OBJECTIVE To develop a preliminary clinical decision guideline, using characteristics of ED pediatric patients presenting with seizures, that successfully predicts all abnormal results of computed tomography (CT) of the head. METHODS We assembled a retrospective case series in the ED of a tertiary

A 6-Month-Old Girl with Incontinentia Pigmenti Presenting as Status Epilepticus.

Ainult registreeritud kasutajad saavad artikleid tõlkida
Logi sisse
Incontinentia pigmenti (IP) is an uncommon neurocutaneous syndrome. Its initial diagnosis is based primarily on characteristic papulovesicular skin lesions and early-onset neonatal seizures. In contrast to typical early neurologic manifestations, we encountered a normally developed 6-month-old

Variations in herpes zoster manifestation.

Ainult registreeritud kasutajad saavad artikleid tõlkida
Logi sisse
Herpes zoster (HZ) is a neurocutaneous disorder due to endogenous reactivation of the varicella-zoster virus (VZV). The typical clinical manifestation is an acute segmental eruption of herpetiform umbilicated vesicles associated with malaise, pain, dysaesthesia, allodynia and probably fever. This
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