Abstract
A 3 week old boy presented with abnormal thyroid function, and was treated with thyroxine. He developed multisystem disease including deafness and nephrotic syndrome, and died aged 3 months. Carbohydrate deficient glycoprotein syndrome (CDGS) was diagnosed post-mortem. CDGS should be considered in all infants with apparently unrelated multiple clinical or biochemical abnormalities.
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- Clayton P. T., Winchester B. G., Keir G. Hypertrophic obstructive cardiomyopathy in a neonate with the carbohydrate-deficient glycoprotein syndrome. J Inherit Metab Dis. 1992;15(6):857–861. doi: 10.1007/BF01800221. [DOI] [PubMed] [Google Scholar]
- Jaeken J., Carchon H., Stibler H. The carbohydrate-deficient glycoprotein syndromes: pre-Golgi and Golgi disorders? Glycobiology. 1993 Oct;3(5):423–428. doi: 10.1093/glycob/3.5.423. [DOI] [PubMed] [Google Scholar]
- Jaeken J., Carchon H. The carbohydrate-deficient glycoprotein syndromes: an overview. J Inherit Metab Dis. 1993;16(5):813–820. doi: 10.1007/BF00714272. [DOI] [PubMed] [Google Scholar]
- Strøm E. H., Strømme P., Westvik J., Pedersen S. J. Renal cysts in the carbohydrate-deficient glycoprotein syndrome. Pediatr Nephrol. 1993 Jun;7(3):253–255. doi: 10.1007/BF00853211. [DOI] [PubMed] [Google Scholar]