Fanconi syndrome in children

Fanconi syndrome (Fanconi syndrome), aliases: Pediatric Syndrome, Pediatric Deb's Blood Deficiency, Pediatric Fanconi Syndrome, Pediatric Fanconi Syndrome, Pediatric Fanconi Blood Deficiency, Pediatric Fanconi Syndrome Syndrome, pediatric compound renal tubular transport deficiency. It is due to the reabsorption of various substances by the proximal tubule, and a large amount of amino acids, glucose, phosphate, bicarbonate and other substances are lost from the urine, resulting in proximal tubule acidosis, hypokalemia, rickets, bone A syndrome of sparseness and retarded growth. Fanconi syndrome can be divided into congenital or acquired, primary or secondary, complete or incomplete. It is relatively rare clinically, with slow onset, and more symptoms than young adults. The prognosis is related to the treatment sooner or later and the response to treatment.

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