Fanconi Syndrome Latest Advances

Journal: Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA

Published: August 20, 2025

Dual-Genetic Etiology in an Atypical Dent Disease Phenotype Which Combines Features of Focal Segmental Glomerulosclerosis and Ellis-Van Creveld-Like Syndrome: A Case Report.

Journal: Case reports in nephrology and dialysis

Published: July 10, 2025

A Case of Hyperinsulinemic Hypoglycaemia Associated with Atypical Fanconi Renal Tubulopathy Syndrome Caused by an HNF4A Variant.

Journal: Case reports in nephrology and dialysis

Published: July 09, 2025

Fanconi Syndrome Latest Advances

Find the Latest Research About Fanconi Syndrome

McCune-Albright Syndrome as a Rare Cause of Fanconi Syndrome and Kidney Failure: A Case Report and Literature Review.

McCune-Albright Syndrome as a Rare Cause of Fanconi Syndrome and Kidney Failure: A Case Report and Literature Review.

Identification of an unusual variant of Fanconi-Bickel syndrome presenting as proximal tubulopathy and short stature.

Identification of an unusual variant of Fanconi-Bickel syndrome presenting as proximal tubulopathy and short stature.

Severe Hypophosphatemia Induced by Hyperventilation: A Case Report.

Severe Hypophosphatemia Induced by Hyperventilation: A Case Report.

Clinical variation in Lowe syndrome: what and how?

Clinical variation in Lowe syndrome: what and how?

Adult-Onset Fanconi Syndrome Presenting as Stress Fractures: A Case Report.

Adult-Onset Fanconi Syndrome Presenting as Stress Fractures: A Case Report.

A Novel Mutation of Fanconi-Bickel Syndrome: A Case Report.

A Novel Mutation of Fanconi-Bickel Syndrome: A Case Report.

Failure to thrive in children with tubulopathies.

Failure to thrive in children with tubulopathies.

Unveiling long-standing low-molecular-weight proteinuria: A proximal tubular mitochondrial enzyme impairment caused by EHHADH mutation.

Unveiling long-standing low-molecular-weight proteinuria: A proximal tubular mitochondrial enzyme impairment caused by EHHADH mutation.

West Nile Virus Neuroinvasive Disease Presenting with Acquired Fanconi Syndrome, Which Resolved on Recovery.

West Nile Virus Neuroinvasive Disease Presenting with Acquired Fanconi Syndrome, Which Resolved on Recovery.

Cadmium toxicity-related metabolic bone disease: a clinical conundrum of five cases.

Cadmium toxicity-related metabolic bone disease: a clinical conundrum of five cases.

Dual-Genetic Etiology in an Atypical Dent Disease Phenotype Which Combines Features of Focal Segmental Glomerulosclerosis and Ellis-Van Creveld-Like Syndrome: A Case Report.

Dual-Genetic Etiology in an Atypical Dent Disease Phenotype Which Combines Features of Focal Segmental Glomerulosclerosis and Ellis-Van Creveld-Like Syndrome: A Case Report.

A Case of Hyperinsulinemic Hypoglycaemia Associated with Atypical Fanconi Renal Tubulopathy Syndrome Caused by an HNF4A Variant.

A Case of Hyperinsulinemic Hypoglycaemia Associated with Atypical Fanconi Renal Tubulopathy Syndrome Caused by an HNF4A Variant.