Pathological and immunological observations in a case of Lesch-Nyhan-syndrome
β Scribed by R. Bassermann; W. Gutensohn; H. Jahn; J. S. Springmann
- Publisher
- Springer
- Year
- 1979
- Tongue
- English
- Weight
- 362 KB
- Volume
- 132
- Category
- Article
- ISSN
- 0340-6997
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β¦ Synopsis
A patient with clearly developed features of the full Lesch-Nyhan syndrome and complete lack of activity of hypoxynthine-phosphoribosyltransferase is described. The clinical picture was characterized by absence of spasticity, good control of autoaggression by behavior therapy, and no signs of renal insufficiency. After death, which was caused by a viral infection, pathological examination and a search for material immunologically crossreacting with hypoxanthine-phosphoribosyltransferase were possible. In spite of increased serum urate levels and raised urinary uric acid excretion there were no signs of urate deposits or damage in the internal organs, including the kidneys. Crossreactive material was found in the liver, kidneys and spleen, a relatively rare finding in the full Lesch-Nyhan-syndrome. The absence of any specific pathological changes in the brain of this patient is in agreement with earlier reports.
π SIMILAR VOLUMES
## Abstract LeschβNyhan disease (LND) is a hereditary disorder of purine metabolism causing severe neurobehavioral disturbances in which an abnormal central nervous system dopaminergic function has been implied. However, levodopa treatment has rarely been used, and reports describe heterogeneous re
## Abstract Extracellular purines have essential roles in neuronal development; hence, disruptions in their metabolism as reported in Lesch Nyhan syndrome (LNS) could result in developmental abnormalities. The deficiency of hypoxanthineβguanine phosphoribosyl transferase (HGPRT) in LNS leads to inc
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