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- KASHIMURA Kimie
- Department of Pediatrics, Jikei University, School of Medicine
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- HIROTSU Takuo
- Department of Pediatrics, Jikei University, School of Medicine
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- AKATSUKA Junichi
- Department of Pediatrics, Jikei University, School of Medicine
Bibliographic Information
- Other Title
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- 遺伝性鉄芽球性貧血の1例
- イデンセイ テツガキュウセイ ヒンケツ ノ 1レイ
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Abstract
A 5 year-old boy with hypochromic anemia and deafness was diagnosed as having hereditary sideroblastic anemia, because hematologic studies revealed hyperferremia and numerous ringed sideroblasts in his bone marrow smears. A similar type of anemia was also found in his uncle who had been diagnosed as a case of primary sideroblastic anemia at another hospital. He did not respond to a large dose of pyridoxal phosphate (200mg/day) administered over several months. Our patient is the youngest case of hereditary sideroblastic anemia ever documented in Japan.
Journal
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- Rinsho Ketsueki
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Rinsho Ketsueki 19 (3), 240-245, 1978
The Japanese Society of Hematology
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Details 詳細情報について
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- CRID
- 1390001205035553024
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- NII Article ID
- 130004497924
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- NII Book ID
- AN00252940
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- COI
- 1:STN:280:CSaD3s%2FgvF0%3D
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- ISSN
- 18820824
- 04851439
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- NDL BIB ID
- 1936643
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- PubMed
- 702810
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- Text Lang
- ja
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- Data Source
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- JaLC
- NDL
- PubMed
- CiNii Articles
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- Abstract License Flag
- Disallowed