| Item type |
[ELS]学術雑誌論文 / Journal Article(1) |
| 公開日 |
2017-01-23 |
| タイトル |
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|
タイトル |
A Case of Hb S/A -α-thalassemia Exhibiting Quadriplegia Due to Distal Renal Tubular Acidosis |
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言語 |
en |
| 言語 |
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|
言語 |
eng |
| 資源タイプ |
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|
資源タイプ識別子 |
http://purl.org/coar/resource_type/c_6501 |
|
資源タイプ |
journal article |
| 著者 |
TAKEMOTO, Yoshinobu
ONO, Hitoshi
KOHAMA, Akitsugu
UEDA, Satoshi
HARANO, Teruo
HARANO, Keiko
SHIBATA, Susumu
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| 著者所属(英) |
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|
en |
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Department of Emergency Medicine, Kawasaki Medical School |
| 著者所属(英) |
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en |
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Department of Rehabilitation Medicine, Kawasaki Medical School |
| 著者所属(英) |
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en |
|
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Department of Emergency Medicine, Kawasaki Medical School |
| 著者所属(英) |
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en |
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Department of Clinical Pathology, Kawasaki Medical School |
| 著者所属(英) |
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en |
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Department of Biochemistry, Kawasaki Medical School |
| 著者所属(英) |
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en |
|
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Department of Biochemistry, Kawasaki Medical School |
| 著者所属(英) |
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|
en |
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Department of Medicine, Kawasaki Medical School |
| キーワード |
|
|
言語 |
en |
|
主題Scheme |
Other |
|
主題 |
distal renal tublar acidosis |
| キーワード |
|
|
言語 |
en |
|
主題Scheme |
Other |
|
主題 |
quadriplegia |
| キーワード |
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|
言語 |
en |
|
主題Scheme |
Other |
|
主題 |
hypopotassemia |
| キーワード |
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|
言語 |
en |
|
主題Scheme |
Other |
|
主題 |
α-thalassemia trait |
| キーワード |
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|
言語 |
en |
|
主題Scheme |
Other |
|
主題 |
sickle cell trait |
| 記事種別(英) |
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|
内容記述タイプ |
Other |
|
内容記述 |
Original Article |
|
言語 |
en |
| 抄録(英) |
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|
en |
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A 46-year-old negro seaman who called at Port Mizushima, Kurashiki City, from West Africa on May 21, 1981 developed quadriplegia shortly after having taken a tablet of an antipyretic agent on the ship. At the Port Clinic in Mizushima, hypopotassemia was detected and Guillain Barre syndrome was suspected. Adrenocorticosteroids therapy was started, but he became dyspneic because of the progression of the paralysis up to the level of respiratory muscle. He was, therefore, transferred to our emergency center and hospitalized. On the sixth hospital day (May 27), clinical manifestations improved by intravenous administration of potassium. Diagnosis of distal renal tubular acidosis was entertained on the basis of the presence of metabolic acidosis, hypopotassemia and the absence of acidification of urine by short duration NH4C1 acid-loading test. The hematological studies revealed a combination of sickle cell trait (Hb S/A) with α-thalassemia trait. It is well known that sickle cell anemia (Hb S/S) occasionally causes secondary distal renal tubular acidosis. However, the occurrence of renal tubular acidosis in sickle cell trait (Hb S/A) and in α-thalassemia trait (αTh/A) has not yet been reported in the literature. It is therefore thought that our observation on this case will deserve special description as one of the possible clinical signs of sickle cell trait. |
| 書誌情報 |
en : Kawasaki medical journal
巻 9,
号 2,
p. 121-129,
発行日 1983
|
| URL |
|
|
識別子 |
http://igakkai.kms-igakkai.com/wp/wp-content/uploads/1983en/9(2)121-129.1983.pdf |
|
識別子タイプ |
URI |
| DOI |
|
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|
識別子タイプ |
DOI |
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|
関連識別子 |
https://doi.org/10.11482/KMJ-E9(2)121 |
| ISSN |
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収録物識別子タイプ |
PISSN |
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収録物識別子 |
0385-0234 |
| ISSN |
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収録物識別子タイプ |
EISSN |
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収録物識別子 |
2434-3404 |
| 雑誌書誌ID |
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収録物識別子タイプ |
NCID |
|
収録物識別子 |
AA00710169 |
| 雑誌書誌ID |
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|
収録物識別子タイプ |
NCID |
|
収録物識別子 |
AA12029005 |
| 著者版フラグ |
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出版タイプ |
VoR |
KJ00010227659.pdf (2.6 MB)
