Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2013 Mar;21(1):26-9.
doi: 10.4250/jcu.2013.21.1.26. Epub 2013 Mar 20.

Fabry cardiomyopathy

Affiliations
Case Reports

Fabry cardiomyopathy

Jae Yong Yoon et al. J Cardiovasc Ultrasound. 2013 Mar.

Abstract

Fabry disease is a progressive X-linked disorder of glycosphingolipid metabolism caused by a deficiency of the α-galactosidase lysosomal enzyme. The partial or complete deficiency of the lysosomal enzyme leads to an accumulation of neutral glycosphingolipids in the vascular endothelium and visceral tissues throughout the body. In the heart, glycosphingolipids deposition causes progressive left ventricular hypertrophy (LVH). We report a case of Fabry disease which was suspected based upon two-dimensional echocardiographic finding of LVH. A 44-year-old man was admitted to evaluation of aggravated exertional dyspnea of two weeks duration. He had been diagnosed with end-stage renal disease of unknown etiology at age 41 followed by renal transplantation that year. He had been treated with oral immunosuppressive agents. On hospital day two, transthoracic echocardiography revealed concentric LVH. Left ventricular systolic function was preserved but diastolic dysfunction was present. Fabry disease was confirmed by demonstration of a low plasma α-galactosidase A (α-Gal A) activity. Analysis of genomic DNA showed α-Gal A gene mutation. The patient was diagnosed with Fabry disease.

Keywords: Alpha-galactosidase A; Cardiomyopathies; Fabry disease.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
The initial electrocardiogram showed left ventricular hypertrophy with a strain pattern, ST-T changes in leads II, III, aVF, V3-V6.
Fig. 2
Fig. 2
Chest radiography. Chest radiography demonstrated cardiomegaly (cardiothoracic ratio = 70%) and blunting of both costophrenic angle.
Fig. 3
Fig. 3
Two dimensional echocardiography. Severe concentric left ventricular hypertrophy is shown in a parasternal long-axis view. The interventricular septal dimension (A) was 23 mm and the left ventricular posterior wall dimension (B) was 22.8 mm in thickness.
Fig. 4
Fig. 4
Pulse-waved Doppler echocardiography (A) and tissue Doppler echocardiography (B). Decreased mitral annulus velocities (E') and increased mitral peak Doppler E-wave (E) to peak mitral annulus velocity ratio (E/E') are seen, suggesting a pseudonormal pattern.

References

    1. Desnick RJ, Ioannou YA, Eng CM. α-galactosidase A deficiency: Fabry disease. In: Scriver CR, Beaudet AL, Sly WS, Valle D, editors. The metabolic and molecular bases of inherited disease. 8th ed. New York: McGraw-Hill; 2001. pp. 3733–3774.
    1. Tanaka H, Adachi K, Yamashita Y, Toshima H, Koga Y. [Four cases of Fabry's disease mimicking hypertrophic cardiomyopathy] J Cardiol. 1988;18:705–718. - PubMed
    1. Jeong JW. Hypertrophic cardiomyopathy. Korean Circ J. 2002;32:7–14.
    1. Eng CM, Guffon N, Wilcox WR, Germain DP, Lee P, Waldek S, Caplan L, Linthorst GE, Desnick RJ International Collaborative Fabry Disease Study Group. Safety and efficacy of recombinant human alpha-galactosidase A--replacement therapy in Fabry's disease. N Engl J Med. 2001;345:9–16. - PubMed
    1. Weidemann F, Breunig F, Beer M, Sandstede J, Turschner O, Voelker W, Ertl G, Knoll A, Wanner C, Strotmann JM. Improvement of cardiac function during enzyme replacement therapy in patients with Fabry disease: a prospective strain rate imaging study. Circulation. 2003;108:1299–1301. - PubMed

Publication types