「超十代オーディション2017」グランプリ受賞で大注目の小貫莉奈ちゃんの撮りおろしデジタル写真集第1弾!ショートカットの美少女です♪「Girls Award 2017」にも出演し、これからいろいろな方面で活躍が期待されてます!本作の撮影は千葉県南房総市の全面協力のもと行われました!作中では得意のバスケ(バリバリの高校バスケ現役!)も見せてくれてます♪すらりと伸びた手足とちっちゃなお顔でスタイル抜群♪写真集第2弾も準備中なのでご期待ください!

『PROTO STAR』 これからの活躍が大いに期待できる美少女を撮りおろしたデジタル写真集シリーズ!
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Publisher
JUPIMAR
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Pages
65
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Language
Japanese
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Genres
Photography / Subjects & Themes / Celebrity
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Among nonsymptomatic epilepsies exhibiting several types of generalized seizures in children two syndromes were progressively identified: epilepsy with myoclonic–astatic seizures (MAE) and nonsymptomatic Lennox–Gastaut syndrome (LGS). Various approaches based on etiology, electroclinical semiology, and mathematical analysis have progressively helped to distinguish these two conditions. Both conditions preferentially affect boys. The course is stereotyped in MAE, characterized by progressive worsening of epilepsy, usual pharmacoresistance at onset and tonic–clonic seizures, myoclonus and frequent episodes of myoclonic status epilepticus. EEG shows 3Hz spike wave bursts characteristic of idiopathic generalized epilepsy together with slowing of the tracing. In LGS, major seizures are mainly atypical absences and tonic seizures with 0.5–2Hz slow spike-waves and eventually focal anomalies. Prognosis in both syndromes ranges from recovery without sequelae to pharmacoresistant epilepsy that has improved over the past 2 decades with the new generation antiepileptic compounds. Iatrogenic factors may contribute to the poor prognosis, mainly in MAE. Pathophysiology remains speculative for both syndromes: although both share factors of brain maturation, MAE is probably mainly related to genetic predisposition whereas LGS results from some unidentified cortical brain malformation. In unfavorable cases, there may therefore be a continuum between both syndromes. They need to be distinguished from other epilepsy syndromes and inborn errors of metabolism that begin in the same age range: atypical idiopathic benign epilepsy, frontal lobe epilepsy with secondary bisynchrony, ring chromosome 20, ceroid lipofuscinosis, and nonsymptomatic late-onset spasms.
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