Haematological findings in type Ib glycogen storage disease before and after portacaval shunt
β Scribed by L. Corbeel; M. Boogaerts; G. Berghe; M. C. Everaerts; G. Marchal; R. Eeckels
- Publisher
- Springer
- Year
- 1983
- Tongue
- English
- Weight
- 386 KB
- Volume
- 140
- Category
- Article
- ISSN
- 0340-6997
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β¦ Synopsis
Persistent neutropenia and repeated respiratory infections were documented in a girl with glycogen storage disease type Ib. A termino-lateral portacaval shunt resulted in normalisation of the granulocyte counts and disappearance of the recurrent infections. The platelet dysfunction that was apparent before surgery, was also corrected by the shunting procedure. A marked hypochromic anaemia, however, probably caused by a sequestration of iron in the spleen and resistant to therapy, remains a persistent feature in this patient.
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## Abstract ## Purpose The aim of this study was to document the sonographic appearance and dimensions of the liver and spleen in patients affected by type I glycogen storage disease and to correlate those findings with laboratory data to evaluate the potential role of sonography in diagnosing tha
## Abstract Glycogen storage disease type Ib is an autosomal recessive inherited metabolic disorder resulting from deficiency of the microsomal glucoseβ6βphosphatase enzyme system. Six patients (three of which were treated with granulocyte colony stimulating factor) suffering from this disease were