Total: 1 |
|
PMID (PMCID) | ||
---|---|---|
25154231 |
MALE | Child |
[Clinical examination of renal function in Cockayne syndrome]. | ||
Motojima T, Sugita K, Omata T, Fujii K. No To Hattatsu. 2014;46(4):311-4. |
||
Cockayne syndrome (CS) is a rare hereditary disease, characterized by profound postnatal brain and somatic growth failure and by the degeneration of multiple tissues resulting in cachexia, dementia, and premature aging. |