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De Toni-Debre-Fanconi Syndrome

Known as: deToni Fanconi syndrome, Toni-Debre-Fanconi Syndrome, Idiopathic De Toni-Debre-Fanconi Syndrome 
A genetic disorder characterized by impairment of the function of the proximal tubules of the kidney, which results in decreased reabsorption of… 
National Institutes of Health

Related topics

Related topics

4 relations
Adult Fanconi syndromeCytochrome-c Oxidase DeficiencyFanconi Syndrome

Broader (1)

Syndrome

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2005
2005
Hypophosphataemic osteomalacia due to de Toni-Debre-Fanconi syndrome in a 19-year old girl.
Osteomalacia associated with adult onset Fanconi syndrome is thought to result from hypophosphataemia due to renal phosphate loss… 
2002
2002
Pattern and associated factors of the neurolathyrism epidemic in Ethiopia
OBJECTIVES To describe the neurolathyrism epidemic in Ethiopia and to identify associated household factors. 
2002
2002
Effect of Grazing on Plant Attributes and Hydrological Properties in the Sloping Lands of the East African Highlands
Extending livestock grazing to the steep slopes has led to unstable grazing systems in the East African Highlands, and new… 
2000
2000
Feed intake, sperm output and seminal characteristics of Ethiopian highland sheep supplemented with different levels of leucaena (Leucaena leucocephala) leaf hay
1998
1998
The house that race built : original essays by Toni Morrison, Angela Y. Davis, Cornel West, and others on Black Americans and politics in America today
Highly Cited
1997
Highly Cited
1997
Utilization of browse supplements with varying tannin levels by Ethiopian Menz sheep: 1. Intake, digestibility and live weight changes
The effect of tannins in browse supplements on intake, digestibility and live weight changes was evaluated using sixty-six male… 
1997
1997
Utilization of browse supplements with varying tannin levels by Ethiopian Menz sheep: 2. Nitrogen metabolism
The effect of different condensed tannins concentrations on protein metabolism from browse supplements was investigated in a 90… 
1996
1996
Sequence variations in the Fanconi anaemia gene, FAC: pathogenicity of 1806insA and R548X and recognition of D195V as a polymorphic variant
Abstract Fanconi anaemia (FA) is a rare autosomal recessive disorder associated with diverse clinical symptoms, increased… 
Review
1977
Review
1977
Limb anomalies in chromosomal aberrations.
This survey shows that there are at least 6 autosomal and 2 gonosomal aberrations which may produce specific types of limb… 
1960
1960
De Toni-Debre-Fanconi syndrome in nephrotic children.
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