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アイテム

  1. Public
  2. 研究紀要
  3. ACTA MEDICA KINDAI UNIVERSITY
  4. 29(2)2004

A child with nail-patella syndrome including nephropathy, autism, and epilepsy

https://kindai.repo.nii.ac.jp/records/2002828
https://kindai.repo.nii.ac.jp/records/2002828
1f491fea-6835-48aa-a1b5-74c442c43b34
名前 / ファイル ライセンス アクション
AA0050842X-20041200-0039.pdf AA0050842X-20041200-0039.pdf (732.5 KB)
アイテムタイプ 紀要論文 / departmental bulletin paper(1)
公開日 2025-05-09
タイトル
タイトル A child with nail-patella syndrome including nephropathy, autism, and epilepsy
言語 en
作成者 Sugimoto, Keisuke

× Sugimoto, Keisuke

en Sugimoto, Keisuke
Kinki University

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Yanagida, Hidehiko

× Yanagida, Hidehiko

en Yanagida, Hidehiko
Kinki University

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Yagi, Kazuro

× Yagi, Kazuro

en Yagi, Kazuro
Kinki University

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Tabata, Nobutada

× Tabata, Nobutada

en Tabata, Nobutada
Kinki University

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Okada, Mitsuru

× Okada, Mitsuru

en Okada, Mitsuru
Kinki University

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Takemura, Tsukasa

× Takemura, Tsukasa

en Takemura, Tsukasa
Kinki University

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言語
言語 eng
キーワード
主題 nail-patella syndrome, nephropathy, autism, epilepsy
内容記述
内容記述タイプ Abstract
内容記述 Nail-Patella syndrome is characterized by dysplasia or absence of nailbeds and patellae, abnormalities of the elbow such as subluxation of the radial head, hornlike overgrowths of the iliac bones, and in some cases, nephropathy. We describe a 3-year-old boy with nail-patella syndrome (NPS) complicated with nephropathy who also had autism and epilepsy. (Patient) He showed signs of autism in a developmental checkup at 1.5 years ; at 2 years, he had his first seizure. The patient's mother had NPS with nephropathy. Proteinuria and hematuria were detected in the boy at 2 years during annual screening. He showed moderate proteinuria, while renal function remained normal. A renal biopsy specimen showed a mild mesangial increase and focal thickening of the glomerular basement membrane (GBM), without immunofluorescence for immunoglobulins or complement components. Ultrastructural examination revealed the characteristics of NPS nephropathy : a slightly thickened GBM with an electron-lucent area ("moth eaten" appearance), and accumulation of coarsely banded collagenous materials. Steroid therapy failed to decrease proteinuria. Nail dysplasia with a triangular lunula was evident mainly in the thumbs, while the patella showed ossification delay. Whether or not the patient's neuropsychiatric disorders are related to NPS remains uncertain. Continued follow-up of nephropathy as well as management of neuropsychiatric manifestations may be required for preventing progression of these complications.
言語 en
出版者
出版者 The Kinki University Medical Association
言語 en
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ departmental bulletin paper
出版タイプ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
収録物識別子
収録物識別子タイプ PISSN
収録物識別子 03866092
開始ページ
開始ページ 39
終了ページ
終了ページ 43
書誌情報 en : ACTA MEDICA KINKI UNIVERSITY

巻 29, 号 2, p. 39-43, 発行日 2004-12
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