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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
1983-2-25
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pubmed:abstractText |
Most of the hereditary sideroblastic anaemias are inherited as x-linked recessive traits and are often pyridoxine responsive. The present paper describes the classical features of sideroblastic anaemia in 2 male and 2 female siblings of a Libyan family. All 4 children had severe anaemia and moderate hepato-splenomegaly. The equal severity of the disease in all 4 family members suggests autosomal inheritance.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:issn |
0001-5792
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
68
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
321-4
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:6817577-Anemia, Sideroblastic,
pubmed-meshheading:6817577-Bone Marrow,
pubmed-meshheading:6817577-Child,
pubmed-meshheading:6817577-Child, Preschool,
pubmed-meshheading:6817577-Erythrocytes, Abnormal,
pubmed-meshheading:6817577-Female,
pubmed-meshheading:6817577-Humans,
pubmed-meshheading:6817577-Iron,
pubmed-meshheading:6817577-Libya,
pubmed-meshheading:6817577-Male,
pubmed-meshheading:6817577-Pyridoxine
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pubmed:year |
1982
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pubmed:articleTitle |
Hereditary sideroblastic anaemia in 4 siblings of a Libyan family--autosomal inheritance.
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pubmed:publicationType |
Journal Article,
Case Reports
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