Abstract
Mutation in the cytokine receptor-like factor 1 and the cardiotrophin-like cytokine ( CRLF1 or CLCF1 genes) phenotypically presents as cold induced sweating syndrome (CISS), which is a rare autosomal recessive disorder. The syndrome is characterized by paradoxical sweating in cold weather, dysmorphic facial features, musculoskeletal deformities, difficulty in feeding, and unexplained recurrent episodes of high-grade fever. We are presenting the first case of CISS with urinary system anomaly, which might relate to CRLF1/CLCF1 complex role in the embryonal nephrogenesis.
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CITATION STYLE
Aljabari, S., Howard, E., Bell, T., & Vasylyeva, T. L. (2013). Cold Induced Sweating Syndrome with Urinary System Anomaly Association. Case Reports in Pediatrics, 2013, 1–4. https://doi.org/10.1155/2013/173890
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