Echocardiographic Features in Familial Amyloidosis with Polyneuropathy
- 12 January 1983
- journal article
- research article
- Published by Wiley in Acta Medica Scandinavica
- Vol. 214 (4), 273-278
- https://doi.org/10.1111/j.0954-6820.1983.tb10634.x
Abstract
Patients (22) with the Swedish variant of familial amyloidosis with polyneuropathy were studied by M-mode and 2-dimensional echocardiography. These patients had few symptoms consistent with cardiac disease but, nevertheless, echocardiograms of only 2 of them, both with a short history of the disease, were considered normal in all aspects. The most common abnormality was increased thickness of the interventricular septum found in 20 (91%) of the patients. This septal hypertrophy was asymmetric in 12 (55%) of them. Two-dimensional echocardiography revealed a characteristic hyperrefractile appearance of the myocardium in 15 (68%) of the patients. Thus, the echocardiography showed a characteristic pattern in these patients. Apparently, cardiac amyloidosis can be diagnosed in the preclinical, asymptomatic state by M-mode and 2 dimensional echocardiography.Keywords
This publication has 15 references indexed in Scilit:
- Pulmonary Function in Familial Amyloidosis with PolyneuropathyActa Medica Scandinavica, 1981
- M-mode and two-dimensional echocardiographic features in cardiac amyloidosis.Circulation, 1981
- Atrioventricular and Intraventricular Conduction in Familial Amyloidosis with PolyneuropathyActa Medica Scandinavica, 1980
- Noninvasive cardiovascular findings in familial amyloid polyneuropathy.Heart, 1978
- Conduction Disturbances in 190 Patients with Familial Amyloidotic Polyneuropathy (Andrade s Type)Published by S. Karger AG ,1977
- Primary Neuropathic Amyloidosis in Three BrothersBMJ, 1974
- Evaluation of Left Ventricular Function by EchocardiographyCirculation, 1972
- Clinically significant cardiac amyloidosisThe American Journal of Cardiology, 1970
- HEREDITARY AMYLOIDOSIS WITH POLYNEUROPATHYActa Medica Scandinavica, 1970
- A PECULIAR FORM OF PERIPHERAL NEUROPATHYBrain, 1952