Emery-Dreifuss muscular dystrophy is a rare disorder characterized by childhood onset of
contractures, humeroperoneal muscle atrophy, and cardiac conduction abnormalities. This …

We reported the autopsy findings in a 50-year-old man with typical clinical features of Emery-
Dreifuss muscular dystrophy. Special attention was directed to the spinal cord and ventral …

We report six patients with Emery-Dreifuss muscular dystrophy (EDMD) and four patients
including one female with EDMD phenotype (EDMDP). This series includes one sporadic …

This report describes two patients, a father and son, with autosomal dominant Emery-
Dreifuss muscular dystrophy. Although the father had the common phenotype, the son had a …

• A 38-year-old woman, a product of consanguineous parents, had been observed to have
limited neck flexion and elbow joints contracture since early childhood. In addition, she …

A 32-year-old woman is described as having the following characteristics of Emery-Dreifuss
muscular dystrophy: humeroperoneal muscular atrophy and weakness, neck and elbow …

A man had weakness of humeroperoneal distribution associated with limited range of
motion of the cervical spine and elbows. At age 25 he developed permanent atrial paralysis …

Clinical and laboratory data of five cases of Emery—Dreifuss muscular dystrophy in three
generations of a family are reported. Severity of the myopathic picture varied in the five …

Emery-Dreifuss dystrophy, an X-linked disorder, is a recently recognized distinct
neuromuscular disease with special pediatric implications. We describe three affected boys …

We report on a man that had weakness of humeroperoneal distribution associated with
limited range of motion of the cervical spine and elbows since he was 5 years old. At age 26 …