Partnership, step by step: a practical model of partnership formation.

Clinical and magnetic resonance image findings of a chronic infantile type patient heterozygous for a nonsense mutation and a large deletion of alpha-L-fucosidase are described and the low intensities of basal ganglia on T2-weighted images seems characteristic of lesions in fucOSidosis.

Abstract

Fucosidosis is a rare autosomal recessive disorder resulting from a deficiency of alpha-L-fucosidase. In this report, we describe clinical and magnetic resonance image (MRI) findings of a chronic infantile type patient heterozygous for a nonsense mutation and a large deletion. The disease onset occurred at 2-3 years of age. She was bound to a wheelchair at 6 years of age, and developed dystonia at the age of 13 years. Brain MRI at 13 years of age showed marked cerebral and cerebellar atrophy, high intensities in the white matter of the frontal and occipital lobes, and low intensities of the bilateral thalamus, striatum, substantia nigra, red nucleus and mamillary bodies on T2-weighted images. The low intensities of basal ganglia on T2-weighted images seems characteristic of lesions in fucosidosis.