Hereditary primary Fanconi disease
Overview
Hereditary primary Fanconi disease: A rare inherited disorder characterized by defective reabsorption of various substances such as phosphate, potassium, amino acids and glucose which manifests as a wide range of abnormalities and problems.
Symptoms
The list of signs and symptoms mentioned in various sources for Hereditary primary Fanconi disease includes the 18 symptoms listed below: * Failure to thrive * Vomiting * Unexplained fever * Excessive urination * Dehydration * Rickets * Osteomalacia * Swan-neck kidney deformity * Kidney lesions * Pyelonephritis * Kidney fibrosis * Kidney vacuolization * Liver cirrhosis * Chronic acidosis * Hypokalemia * Excess sugar in the urine * Excess phosphates in urine * Excess amino acids in urine Note that Hereditary primary Fanconi disease symptoms usually refers to various symptoms known to a patient, but the phrase Hereditary primary Fanconi disease signs may refer to those signs only noticable by a doctor.
Causes
* Chronic acidosis * Dehydration * Excess amino acids in urine * Excessive urination * Failure to thrive * Hypokalemia * Kidney fibrosis * Liver cirrhosis * Pyelonephritis * Rickets * Unexplained fever * Vomiting
Diagnosis
The signs and symptom information on this page attempts to provide a list of some possible signs and symptoms of Hereditary primary Fanconi disease. This medical information about signs and symptoms for Hereditary primary Fanconi disease has been gathered from various sources, may not be fully accurate, and may not be the full list of Hereditary primary Fanconi disease signs or Hereditary primary Fanconi disease symptoms. Furthermore, signs and symptoms of Hereditary primary Fanconi disease may vary on an individual basis for each patient. Only your doctor can provide adequate diagnosis of any signs or symptoms and whether they are indeed Hereditary primary Fanconi disease symptoms.