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PedAM

Pediatric Disease Annotations & Medicines




Disease ataxia
Phenotype C1527336|sjogren syndrome
Sentences 3
PubMedID- 19801575 Mutations in the sil1 gene have been associated with marinesco-sjogren syndrome, hallmarks of which include ataxia and cerebellar atrophy.
PubMedID- 22849991 His sensory ataxia might be attributed to sjogren syndrome-associated ganglionopathy at the cervical level, and the mri findings might reflect centripetal wallerian degeneration in the cuneate fasciculus.
PubMedID- 19801575 Mutations in the sil1 gene have been associated with marinesco–sjögren syndrome, hallmarks of which include ataxia and cerebellar atrophy.

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