Renal amyloidosis is a detrimental disease caused by the deposition of amyloid fibrils. A child with renal amyloidosis may present with proteinuria or nephrotic syndrome. Chronic renal failure may follow. Amyloid fibrils may deposit in other organs as well. The diagnosis is through the typical appearance on histopathology. Although chronic infections and chronic inflammatory diseases used to be the causes of secondary amyloidosis in children, the most frequent cause is now autoinflammatory diseases. Among this group of diseases, the most frequent one throughout the world is familial Mediterranean fever (FMF). FMF is typically characterized by attacks of clinical inflammation in the form of fever and serositis and high acute-phase reactants....
International audienceWe retrospectively reviewed the clinicopathological features of a series of 68...
Amyloidosis is a protein misfolding disorder in which soluble proteins aggregate as insoluble amyloi...
International audienceWe retrospectively reviewed the clinicopathological features of a series of 68...
Hereditary amyloidoses with renal involvement are classified in two groups. The first group is a gro...
Amyloidosis is a disorder in which soluble proteins aggregate and are deposited extracellularly in t...
Amyloidosis is a disorder in which soluble proteins aggregate and are deposited extracellularly in t...
Amyloidosis is a heterogeneous group of hereditary and acquired diseases in which normally soluble p...
PubMedID: 10755352We studied a group of 59 patients with renal amyloidosis. Mean age (45 male, 14 fe...
Familial Mediterranean Fever (FMF) is the most prevalent monogenic hereditary autoinflammatory disea...
PubMedID: 16570202The kidney is frequently affected in patients with sickle cell syndrome, i.e., hom...
We studied a group of 59 cases with renal amyloidosis. Mean age (45 male, 14 female) was 33.05±13.04...
Renal amyloidoses are a group of rare misfolding protein diseases caused by the deposition of a prec...
Hereditary periodic fever syndromes are a group of genetic diseases clinically characterized by recu...
Hereditary periodic fever syndromes are a group of genetic diseases clinically characterized by recu...
Abstract: We studied a group of 59 cases with renal amyloidosis. Mean age (45 male, 14 female) was 3...
International audienceWe retrospectively reviewed the clinicopathological features of a series of 68...
Amyloidosis is a protein misfolding disorder in which soluble proteins aggregate as insoluble amyloi...
International audienceWe retrospectively reviewed the clinicopathological features of a series of 68...
Hereditary amyloidoses with renal involvement are classified in two groups. The first group is a gro...
Amyloidosis is a disorder in which soluble proteins aggregate and are deposited extracellularly in t...
Amyloidosis is a disorder in which soluble proteins aggregate and are deposited extracellularly in t...
Amyloidosis is a heterogeneous group of hereditary and acquired diseases in which normally soluble p...
PubMedID: 10755352We studied a group of 59 patients with renal amyloidosis. Mean age (45 male, 14 fe...
Familial Mediterranean Fever (FMF) is the most prevalent monogenic hereditary autoinflammatory disea...
PubMedID: 16570202The kidney is frequently affected in patients with sickle cell syndrome, i.e., hom...
We studied a group of 59 cases with renal amyloidosis. Mean age (45 male, 14 female) was 33.05±13.04...
Renal amyloidoses are a group of rare misfolding protein diseases caused by the deposition of a prec...
Hereditary periodic fever syndromes are a group of genetic diseases clinically characterized by recu...
Hereditary periodic fever syndromes are a group of genetic diseases clinically characterized by recu...
Abstract: We studied a group of 59 cases with renal amyloidosis. Mean age (45 male, 14 female) was 3...
International audienceWe retrospectively reviewed the clinicopathological features of a series of 68...
Amyloidosis is a protein misfolding disorder in which soluble proteins aggregate as insoluble amyloi...
International audienceWe retrospectively reviewed the clinicopathological features of a series of 68...