Familial Amyloidosis with Polyneuropathy was first recognized in Portugal and reported by Andrade in 1952. The disease is rare, but clustering of the patients has been reported from Portugal, Japan and northern Sweden. The gastrointestinal involvement in the Swedish form of the disease was studied in this investigation. In a study of 52 patients on their first admission 47 displayed gastrointestinal symptoms in the form of severely altered bowel habits (intractable diarrhea and/or constipation). Steatorrhea was found in 30 out of 52 patients (58%) and an impaired d-xylose absorption in 26 out of 50 patients (52%). The steatorrhea was correlated to the degree of peripheral polyneuropathy as expressed by EMG-score. No relation could be establ...
Amyloidosis is a disease marked by deposition of misfolded proteins, known as amyloids, in the extra...
Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, p...
Background and Aims: Hereditary transthyretin (ATTRv) amyloidosis represents a diagnostic challenge ...
Purpose: To review the management of gastrointestinal symptoms in patients with hereditary transthyr...
Amyloidosis is a rare disease caused by extracellular deposits of insoluble fibrillar proteins in va...
Amyloidosis is characterized by the accumulation of an insoluble amyloid protein in the extracellula...
Introduction: The systemic amyloidosis usually doesn’t save the digestive tract, but this involvemen...
Amyloidosis is not a single disease but a term for diseases that share a common feature: the extrace...
The authors present a review of 21 cases with the diagnosis of type I amyloid neuropathy based on ep...
The authors present a review of 21 cases with the diagnosis of type I amyloid neuropathy based on ep...
Gastrointestinal (GI) amyloidosis represents a significant diagnostic challenge due to its nonspecif...
Background: Gastrointestinal complications are common in hereditary transthyretin amyloid (ATTRm) am...
Background Few families with autosomal dominant forms of chronic idiopathic pseudo-obstruction (CIP)...
Systemic amyloidosis is a group of complex disorders characterized by the extracellular deposition o...
To report the clinical, pathologic and molecular genetic features of a Chinese family with familial ...
Amyloidosis is a disease marked by deposition of misfolded proteins, known as amyloids, in the extra...
Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, p...
Background and Aims: Hereditary transthyretin (ATTRv) amyloidosis represents a diagnostic challenge ...
Purpose: To review the management of gastrointestinal symptoms in patients with hereditary transthyr...
Amyloidosis is a rare disease caused by extracellular deposits of insoluble fibrillar proteins in va...
Amyloidosis is characterized by the accumulation of an insoluble amyloid protein in the extracellula...
Introduction: The systemic amyloidosis usually doesn’t save the digestive tract, but this involvemen...
Amyloidosis is not a single disease but a term for diseases that share a common feature: the extrace...
The authors present a review of 21 cases with the diagnosis of type I amyloid neuropathy based on ep...
The authors present a review of 21 cases with the diagnosis of type I amyloid neuropathy based on ep...
Gastrointestinal (GI) amyloidosis represents a significant diagnostic challenge due to its nonspecif...
Background: Gastrointestinal complications are common in hereditary transthyretin amyloid (ATTRm) am...
Background Few families with autosomal dominant forms of chronic idiopathic pseudo-obstruction (CIP)...
Systemic amyloidosis is a group of complex disorders characterized by the extracellular deposition o...
To report the clinical, pathologic and molecular genetic features of a Chinese family with familial ...
Amyloidosis is a disease marked by deposition of misfolded proteins, known as amyloids, in the extra...
Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, p...
Background and Aims: Hereditary transthyretin (ATTRv) amyloidosis represents a diagnostic challenge ...