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Первинний ренотубулярний синдром Фанконі

ORPHA:3337· ICD-10 E72.0· Primary Fanconi renotubular syndrome

Визначення(English summary)

A rare generalized, genetic disorder of proximal tubular transport characterized by excessive urine output with loss of low molecular weight solutes (amino acids, glucose, low-molecular weight proteins, organic acids, carnitine, calcium, phosphate, potassium, bicarbonate) and water, and which can be life threatening.

Поширеність
Unknown
Успадкування
Autosomal dominant, Autosomal recessive
Вік початку
Childhood, Infancy