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PedAM

Pediatric Disease Annotations & Medicines




Disease cerebellar degeneration
Phenotype C0009207|cockayne syndrome
Sentences 1
PubMedID- 22411250 First, in our studies on hereditary dna repair disorders, increased oxidative dna damage and lipid peroxidation were carried out in the degeneration of basal ganglia, intracerebral calcification and cerebellar degeneration in patients with xeroderma pigmentosum, cockayne syndrome and ataxia-telangiectasia-like disorder, respectively.

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