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Permanent Neonatal Diabetes Mellitus with Growth Disturbance,Developmental Delay,Epilepsy and Dysmorphic Features

https://asahikawa-med.repo.nii.ac.jp/records/592
https://asahikawa-med.repo.nii.ac.jp/records/592
6f32b820-1882-4d0e-b827-d3661e489e18
名前 / ファイル ライセンス アクション
739.pdf 739.pdf (1.7 MB)
Item type 学術雑誌論文 / Journal Article_02(1)
公開日 2007-10-04
タイトル
タイトル Permanent Neonatal Diabetes Mellitus with Growth Disturbance,Developmental Delay,Epilepsy and Dysmorphic Features
言語 en
言語
言語 eng
資源タイプ
資源タイプ journal article
その他(別言語等)のタイトル
その他のタイトル 成長異常,発育遅延,てんかん,奇異な顔貌を伴った永続型新生児糖尿病(著者の要望によるタイトル) 成長異常,発育遅延,てんかん,奇異な顔貌を伴った恒久的新生児糖尿病(医中誌のタイトル)
著者 鈴木, 滋

× 鈴木, 滋

鈴木, 滋

ja-Kana スズキ, シゲル

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Mukai, Tokuo

× Mukai, Tokuo

Mukai, Tokuo

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Uetake, Kimiaki

× Uetake, Kimiaki

Uetake, Kimiaki

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Sageshima, Syun-ichi

× Sageshima, Syun-ichi

Sageshima, Syun-ichi

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Matsuo, Kumihiro

× Matsuo, Kumihiro

Matsuo, Kumihiro

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Ueda, Osamu

× Ueda, Osamu

Ueda, Osamu

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Ito, Yoshiya

× Ito, Yoshiya

Ito, Yoshiya

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Fujieda, Kenji

× Fujieda, Kenji

Fujieda, Kenji

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著者 ローマ字
Suzuki, Shigeru
書誌情報 Clinical Pediatric Endocrinology

巻 14, 号 suppl.24, p. 81-84, 発行日 2005-12-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 0918-5739
抄録
内容記述タイプ Abstract
内容記述 We report the case of 15-mo-old girl who manifested neonatal diabetes mellitus associated with IUGR, developmental delay, epilepsy dysmorphic features and growth disturbance. She was born at 38 wk of gestation after normal pregnancy. Her birth weight was 2262 g (<10%tile) and height 45.0 cm (<10%tile). Since birth she gradually presented failure to thrive and presented hyperglycemia (glucose 692 mg/dl), ketoacidosis and elevated HbA1c level (7.7%) at 3 mo of age. The anti-GAD antibody was negative and the serum CPR level was 0.5 ng/ml. The girl was treated with intensive insulin therapy from 3 mo of age, however, her weight did not improve and was only 3305 g (-4.6 SD) at 5 mo of age. When admitted to our hospital, she was recognized as having dysmorphic features such as prominent forehead, downturned mouth, bilateral ptosis, arthrogryposis, hypertonia and umbilical hernia. Because she presented frequent hypoglycemic episodes under the intensive insulin injection regimen, treatment was changed to a twice a day injection schedule. Subsequently, the patient did not show any hypoglycemic episodes and she gradually gained a weight. However, at 7 mo of age, seizures developed and her EEG was hypsarrhythmic. She is now 15 mo of age but she cannot sit without support. She is still short and her height is 64.8 cm (-3.9 SD).
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内容記述タイプ Other
注記 雑誌掲載版
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資源タイプ text
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内容記述 application/pdf
ID(XooNIps)
2006310359
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904
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