Woodhouse-Sakati Syndrome: A Case Section Report from Indonesia
Woodhouse-Sakati Syndrome (WSS) is an extremely rare autosomal recessive neuroendocrine disease with loss of function mutation of DCAF17 gene, located on chromosome 2q31. This report discusses the first documented case of suspected WSS in Indonesia in a 20-year-old female patient with multiple metab...
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| Format: | Article |
| Language: | English |
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JCDR Research and Publications Private Limited
2019-01-01
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| Series: | Journal of Clinical and Diagnostic Research |
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| Online Access: | https://jcdr.net/articles/PDF/12481/38431_CE[Ra1]_F(SHU)_PF1(AB_KM)_PN(SL).pdf |