Abstract
Macroamylasaemia and selective IgA deficiency were diagnosed in a 2 year old child who presented with persistent hyperamylasaemia. Macroamylasaemia is an isolated biochemical abnormality caused by aggregation of serum amylase activity with immunoglobulins. Early recognition of macroamylasaemia is important to avoid diagnosing pancreatic disease.
Full text
PDFImages in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Berk J. E., Kizu H., Take S., Fridhandler L. Macroamylasemia: clinical and laboratory features. Am J Gastroenterol. 1970 Mar;53(3):211–222. [PubMed] [Google Scholar]
- Colón A. R., Felder R. A., Ryan T. M. Macroamylasemia. J Pediatr. 1980 Jan;96(1):64–66. doi: 10.1016/s0022-3476(80)80329-5. [DOI] [PubMed] [Google Scholar]
- Harada K., Nakayama T., Kitamura M., Sugimoto T. Immunological and electrophoretical approaches to macroamylase analysis. Clin Chim Acta. 1975 Mar 24;59(3):291–299. doi: 10.1016/0009-8981(75)90004-2. [DOI] [PubMed] [Google Scholar]
- Tomásová H., Kottová V., Hanák J., Kamarýt J. Makroamylazémie u detí. Cesk Pediatr. 1981 Nov;36(11):643–645. [PubMed] [Google Scholar]
- Warshaw A. L., Lee K. H. Macroamylasemia and other chronic nonspecific hyperamylasemias: chemical oddities or clinical entities? Am J Surg. 1978 Apr;135(4):488–493. doi: 10.1016/0002-9610(78)90025-9. [DOI] [PubMed] [Google Scholar]