An early onset Gitelman syndrome presenting in a boy with failure to thrive with recurrent hypokalemia and hypomagnesemia: a case report.

Gitelman syndrome is an autosomal recessive, chronically salt-losing tubulopathy depicted by renal potassium wasting, hypokalemia, hypocalciuric, hypomagnesemia, metabolic alkalosis, and hyperreninemic hyperaldosteronism with average or low blood pressure. This case report describes a 10-year-old boy who presented with acute respiratory tract infection with respiratory distress, myalgia, generalized muscle weakness, and significant biochemical changes like hypokalemia, hypomagnesemia, and metabolic alkalosis associated with failure to thrive. Further investigations, like genetic testing, showed a SLC12A3 gene mutation, a pathogenic homozygosity variant, proving the diagnosis of Gitelman syndrome.

Fuzzy segmentation and black widow-based optimal SVM for skin disease classification.

The skin, which has seven layers, is the main human organ and external barrier. According to the World Health Organization (WHO), skin cancer is the fourth leading cause of non-fatal disease risk. In medicinal fields, skin disease classification is a major challenging issue due to inaccurate outputs, overfitting, larger computational cost, and so on.