De Toni Debre Fanconi syndrome is the name given to a genetic disease. It involves reabsorption of various substances in the kidney. What is de Toni Debre Fanconi syndrome? De Toni-Debre-Fanconi syndrome is also known as De Toni-Debre-Fanconi complex, De Toni-Fanconi syndrome, or glucose-amino acid diabetes. This refers to a renal resorption disorder of the … De Toni Debre Fanconi Syndrome: Causes, Symptoms & Treatment
Aminoaciduria refers to a number of diseases and metabolic disorders that result in the excretion of amino acids through the final urine. In most cases, this is hyperaminoaciduria, in which more than 5 percent of the amino acids that have been filtered through the renal corpuscles into the primary urine are not reabsorbed and therefore … Aminoaciduria: Causes, Symptoms & Treatment
Pearson syndrome is a very rare disease with genetic causes. The disease is also known as Pearson’s disease among some medical professionals. The hereditary disease belongs to the so-called mitochondriopathies. Pearson’s syndrome is characterized by multisystemic complaints. The disease is typically characterized by deletion of mitochondrial DNA. What is Pearson syndrome? Pearson syndrome represents a … Pearsons Disease: Causes, Symptoms & Treatment
Fanconi-Bickel syndrome is a disorder in which glycogen storage is impaired. The disease is very rare and is synonymously referred to as glycogenosis type XI or Bickel-Fanconi glycogenosis. The disease is due to a defect on the gene ‘GLUT-2’. What is Fanconi-Bickel syndrome? In Fanconi-Bickel syndrome, glycogen storage in the kidneys and liver is impaired. … Fanconi-Bickel Syndrome: Causes, Symptoms & Treatment
