Publications by authors named "T Saideekshit"
Isochromosome mosaic Turner syndrome (IMTS) is a rare genetic variant of Turner syndrome (TS). The diagnosis of TS can be missed until adolescence or early adulthood in females with minimal symptoms. The clinical features of mosaic TS can be atypical and should be evaluated thoroughly to detect potential complications.
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- - Wolfram syndrome (WFS) is a rare genetic disorder causing neurodegenerative symptoms like diabetes, vision and hearing loss, and various other complications.
- - A 22-year-old male with a history of type 1 diabetes developed optic nerve degeneration and sensorineural hearing loss, alongside symptoms of diabetes insipidus and polydipsia.
- - After thorough evaluation and genetic testing, he was diagnosed with WFS and is currently treated with insulin and desmopressin for his conditions.