Fabry's disease with familial lymphedema of the lower limbs. Case report and family study

European Neurology
F GemignaniM Savi

Abstract

The case of a 49-year-old man with Fabry's disease (FD), confirmed by histopathological findings of kidney and skin biopsies and enzymatic studies, is reported. Clinical symptoms mainly consisted in severe neurological involvement, and in conspicuous lymphedema of the lower limbs. Two decreased brothers of the patient were also affected with symptons strongly suggesting FD, as well as the lymphedema of the lower limbs. On the basis of these data, the association of FD with familial lymphedema of the lower limbs is discussed: a lipid accumulation in the lymphatic as well as the blood vessel wall is proposed as a possible explanation; the hypothesis of an inborn error in the development of the lymphatic system, controlled by a gene closedly associated with the FD gene on the same chromosome can also be advanced.

Citations

Feb 17, 2006·Genetics in Medicine : Official Journal of the American College of Medical Genetics·Markus RiesDonna Krasnewich
Jan 1, 1982·Acta Neuropathologica·F TagliaviniA Federico
Oct 29, 2002·Muscle & Nerve·Carlos A LucianoRaphael Schiffmann
Dec 19, 2002·Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society·M DütschM J Hilz
Mar 12, 2003·American Journal of Clinical Dermatology·Matthias MöhrenschlagerDietrich Abeck
Sep 24, 2004·The Journal of Comparative Neurology·Edward V Famiglietti

Related Concepts

Fabry Disease
Cerebroside-Sulfatase
Galactosidase
Glucosidase
Glucosaminidases
Kidney
Leg
Milroy Disease
Genealogical Tree
Skin

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