A metabolic disorder similar to Zellweger syndrome with hepatic acatalasia and absence of peroxisomes, altered content and redox state of cytochromes, and infantile cirrhosis with hemosiderosis. [electronic resource]
Producer: 19770512Description: 261-75 p. digitalISSN:- 0340-6199
- Catalase -- metabolism
- Cytochromes -- analysis
- Diagnosis, Differential
- Endoplasmic Reticulum -- ultrastructure
- Hemosiderosis -- diagnosis
- Humans
- Infant
- Liver -- enzymology
- Liver Cirrhosis -- diagnosis
- Male
- Metabolism, Inborn Errors -- diagnosis
- Microbodies -- ultrastructure
- Microscopy, Electron
- Mitochondria, Liver -- ultrastructure
- Muscle Spasticity -- diagnosis
- Syndrome
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Publication Type: Case Reports; Journal Article
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