WEKO3
アイテム
{"_buckets": {"deposit": "583cc0ed-7e46-440d-aa78-c693627acf34"}, "_deposit": {"created_by": 2, "id": "3888", "owners": [2], "pid": {"revision_id": 0, "type": "depid", "value": "3888"}, "status": "published"}, "_oai": {"id": "oai:nagasaki-u.repo.nii.ac.jp:00003888", "sets": ["262"]}, "author_link": ["15809", "15810", "15808", "15806", "15804", "15807", "15811", "15805"], "item_3_biblio_info_6": {"attribute_name": "書誌情報", "attribute_value_mlt": [{"bibliographicIssueDates": {"bibliographicIssueDate": "2017-01", "bibliographicIssueDateType": "Issued"}, "bibliographicIssueNumber": "1", "bibliographicPageEnd": "15", "bibliographicPageStart": "9", "bibliographicVolumeNumber": "61", "bibliographic_titles": [{"bibliographic_title": "Acta medica Nagasakiensia"}]}]}, "item_3_description_4": {"attribute_name": "抄録", "attribute_value_mlt": [{"subitem_description": "A 20-year-old woman presented to the Department of Obstetrics and Gynecology of our hospital for a prenatal checkup at 33 weeks’ gestation. No abnormalities had been ever found in routine urine testing at school health checkups. Blood tests revealed renal impairment, with a creatinine level of 1.77 mg/dL, and she was referred to our department. Hematuria and proteinuria were not found; therefore, she was allowed to continue the pregnancy while being followed for renal function. Renal biopsy was performed after delivery. Pathological examination revealed irregular renal tubular dilatation and atrophy associated with thickening, thinning, and disruption of the tubular basement membrane and diffuse fibrosis and cell infiltration in the interstitium. Based on these findings, nephronophthisis was suspected. Genetic analysis revealed complete homozygous deletion of NPHP1, and nephronophthisis was efinitively diagnosed. Currently, the only curative treatment available for nephronophthisis is renal transplantation, and thus, symptomatic treatment for chronic kidney disease eventually becomes necessary. Because nephronophthisis lacks clear clinical symptoms, early diagnosis is difficult. Thus, if young patients present with renal impairment, a detailed examination is necessary to consider nephronophthisis in the differential diagnosis.", "subitem_description_type": "Abstract"}]}, "item_3_description_64": {"attribute_name": "引用", "attribute_value_mlt": [{"subitem_description": "Acta medica Nagasakiensia, 61(1), pp.9-15; 2017", "subitem_description_type": "Other"}]}, "item_3_publisher_33": {"attribute_name": "出版者", "attribute_value_mlt": [{"subitem_publisher": "Nagasaki University School of Medicine"}]}, "item_3_source_id_10": {"attribute_name": "書誌レコードID", "attribute_value_mlt": [{"subitem_source_identifier": "AA00508430", "subitem_source_identifier_type": "NCID"}]}, "item_3_source_id_7": {"attribute_name": "ISSN", "attribute_value_mlt": [{"subitem_source_identifier": "00016055", "subitem_source_identifier_type": "ISSN"}]}, "item_3_text_62": {"attribute_name": "sortkey", "attribute_value_mlt": [{"subitem_text_value": "03"}]}, "item_3_text_63": {"attribute_name": "出版者別言語", "attribute_value_mlt": [{"subitem_text_value": "長崎大学医学部"}]}, "item_3_version_type_16": {"attribute_name": "著者版フラグ", "attribute_value_mlt": [{"subitem_version_resource": "http://purl.org/coar/version/c_970fb48d4fbd8a85", "subitem_version_type": "VoR"}]}, "item_creator": {"attribute_name": "著者", "attribute_type": "creator", "attribute_value_mlt": [{"creatorNames": [{"creatorName": "Oka, Satoru"}], "nameIdentifiers": [{"nameIdentifier": "15804", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Obata, Yoko"}], "nameIdentifiers": [{"nameIdentifier": "15805", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Mori, Atsushi"}], "nameIdentifiers": [{"nameIdentifier": "15806", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Nakazawa, Masayuki"}], "nameIdentifiers": [{"nameIdentifier": "15807", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Morisada, Naoya"}], "nameIdentifiers": [{"nameIdentifier": "15808", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Iijima, Kazumoto"}], "nameIdentifiers": [{"nameIdentifier": "15809", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Mukae, Hiroshi"}], "nameIdentifiers": [{"nameIdentifier": "15810", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Nishino, Tomoya"}], "nameIdentifiers": [{"nameIdentifier": "15811", "nameIdentifierScheme": "WEKO"}]}]}, "item_files": {"attribute_name": "ファイル情報", "attribute_type": "file", "attribute_value_mlt": [{"accessrole": "open_date", "date": [{"dateType": "Available", "dateValue": "2020-12-21"}], "displaytype": "detail", "download_preview_message": "", "file_order": 0, "filename": "ActMed61_9.pdf", "filesize": [{"value": "699.1 kB"}], "format": "application/pdf", "future_date_message": "", "is_thumbnail": false, "licensetype": "license_free", "mimetype": "application/pdf", "size": 699100.0, "url": {"label": "ActMed61_9.pdf", "url": "https://nagasaki-u.repo.nii.ac.jp/record/3888/files/ActMed61_9.pdf"}, "version_id": "a39941bd-b044-4e2e-822f-5c08caf1fa66"}]}, "item_keyword": {"attribute_name": "キーワード", "attribute_value_mlt": [{"subitem_subject": "nephronophthisis", "subitem_subject_scheme": "Other"}, {"subitem_subject": "cystic kidney disease", "subitem_subject_scheme": "Other"}, {"subitem_subject": "polyuria", "subitem_subject_scheme": "Other"}, {"subitem_subject": "hyposthenuria", "subitem_subject_scheme": "Other"}, {"subitem_subject": "gestation", "subitem_subject_scheme": "Other"}, {"subitem_subject": "pregnancy", "subitem_subject_scheme": "Other"}]}, "item_language": {"attribute_name": "言語", "attribute_value_mlt": [{"subitem_language": "eng"}]}, "item_resource_type": {"attribute_name": "資源タイプ", "attribute_value_mlt": [{"resourcetype": "departmental bulletin paper", "resourceuri": "http://purl.org/coar/resource_type/c_6501"}]}, "item_title": "A case of nephronophthisis discovered due to pregnancy with review of literatures", "item_titles": {"attribute_name": "タイトル", "attribute_value_mlt": [{"subitem_title": "A case of nephronophthisis discovered due to pregnancy with review of literatures"}]}, "item_type_id": "3", "owner": "2", "path": ["262"], "permalink_uri": "http://hdl.handle.net/10069/37077", "pubdate": {"attribute_name": "公開日", "attribute_value": "2017-03-16"}, "publish_date": "2017-03-16", "publish_status": "0", "recid": "3888", "relation": {}, "relation_version_is_last": true, "title": ["A case of nephronophthisis discovered due to pregnancy with review of literatures"], "weko_shared_id": 2}
A case of nephronophthisis discovered due to pregnancy with review of literatures
http://hdl.handle.net/10069/37077
http://hdl.handle.net/10069/370776b8bb7db-aba0-4c1f-8772-0fea8f1f6643
名前 / ファイル | ライセンス | アクション |
---|---|---|
ActMed61_9.pdf (699.1 kB)
|
|
Item type | 紀要論文 / Departmental Bulletin Paper(1) | |||||
---|---|---|---|---|---|---|
公開日 | 2017-03-16 | |||||
タイトル | ||||||
タイトル | A case of nephronophthisis discovered due to pregnancy with review of literatures | |||||
言語 | ||||||
言語 | eng | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | nephronophthisis | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | cystic kidney disease | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | polyuria | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | hyposthenuria | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | gestation | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | pregnancy | |||||
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 | |||||
著者 |
Oka, Satoru
× Oka, Satoru× Obata, Yoko× Mori, Atsushi× Nakazawa, Masayuki× Morisada, Naoya× Iijima, Kazumoto× Mukae, Hiroshi× Nishino, Tomoya |
|||||
抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | A 20-year-old woman presented to the Department of Obstetrics and Gynecology of our hospital for a prenatal checkup at 33 weeks’ gestation. No abnormalities had been ever found in routine urine testing at school health checkups. Blood tests revealed renal impairment, with a creatinine level of 1.77 mg/dL, and she was referred to our department. Hematuria and proteinuria were not found; therefore, she was allowed to continue the pregnancy while being followed for renal function. Renal biopsy was performed after delivery. Pathological examination revealed irregular renal tubular dilatation and atrophy associated with thickening, thinning, and disruption of the tubular basement membrane and diffuse fibrosis and cell infiltration in the interstitium. Based on these findings, nephronophthisis was suspected. Genetic analysis revealed complete homozygous deletion of NPHP1, and nephronophthisis was efinitively diagnosed. Currently, the only curative treatment available for nephronophthisis is renal transplantation, and thus, symptomatic treatment for chronic kidney disease eventually becomes necessary. Because nephronophthisis lacks clear clinical symptoms, early diagnosis is difficult. Thus, if young patients present with renal impairment, a detailed examination is necessary to consider nephronophthisis in the differential diagnosis. | |||||
書誌情報 |
Acta medica Nagasakiensia 巻 61, 号 1, p. 9-15, 発行日 2017-01 |
|||||
ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 00016055 | |||||
書誌レコードID | ||||||
収録物識別子タイプ | NCID | |||||
収録物識別子 | AA00508430 | |||||
著者版フラグ | ||||||
出版タイプ | VoR | |||||
出版タイプResource | http://purl.org/coar/version/c_970fb48d4fbd8a85 | |||||
出版者 | ||||||
出版者 | Nagasaki University School of Medicine | |||||
出版者別言語 | ||||||
長崎大学医学部 | ||||||
sortkey | ||||||
03 | ||||||
引用 | ||||||
内容記述タイプ | Other | |||||
内容記述 | Acta medica Nagasakiensia, 61(1), pp.9-15; 2017 |