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.
Versmold, H T
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] - European journal of pediatrics Mar 1977 - 261-75 p. digital
Publication Type: Case Reports; Journal Article
0340-6199
10.1007/BF00441934 doi
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
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] - European journal of pediatrics Mar 1977 - 261-75 p. digital
Publication Type: Case Reports; Journal Article
0340-6199
10.1007/BF00441934 doi
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