Sage Journals: Discover world-class research

Abstract

Get full access to this article

View all access options for this article.

References

Munsat

. Facioscapulohumeral dystrophy and the scapuloperoneal syndrome. In: Engel

Banker

, ed. Myology. New York: McGraw-Hill, 1986: 1251–66.

Kaeser

. Scapuloperoneal muscular atrophy. Brain 1975; 88: 407–18.

Davidenkow

. Scapuloperoneal amyotrophy. Arch Neurol Psychiatry 1939; 41: 694–701.

Allen

. Hearing acuity in patients with muscular dystrophy. Dev Med Child Neurol 1973; 15: 500–5.

Taylor

Caroll

Smith

Johnson

Johnston

Brooke

. Facioscapulohumeral dystrophy associated with hearing loss and Coats syndrome. Ann Neurol 1982; 12: 395–8.

Korf

Bresnan

Shapiro

Sotrel

Abrams

. Facioscapulohumeral dystrophy presenting in infancy with facial diplegia and sensorineural deafness. Ann Neurol 1985; 17: 513–6.

Wulff

Lin

Kepes

. Inflammatory facioscapulohumeral muscular dystrophy and Coats syndrome. Ann Neurol 1982; 12: 398–401.

Meyerson

Lewis

Ill

. Facioscapulohumeral muscular dystrophy and accompanying hearing loss. Arch Otolaryngol 1984; 110: 261–6.

Kuhn

. Labyrinthine deafness in myotonic dystrophy and in progressive muscular dystrophy. Dtsch Med Wochenschr 1966; 91: 947–54.

10.

Monnens

Gabreels

Williams

. A metabolic myopathy associated with chronic lactic acidemia, growth failure, and nerve deafness. J Pediatr 1975; 86: 983.

11.

Paparella

. Sensorineural hearing loss in children—genetic. In: Paparella

Shumrick

, ed. Otolaryngology. 2nd ed. Philadelphia: WB Saunders, 1980: 1718–34.

12.

Monaco

Neve

Colletti-Feener

Bontelson

Kuinot

Kunkel

. Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene. Nature 1986; 323: 646–50.

Autosomal Dominant Scapuloperoneal Syndrome with Sensorineural Hearing Loss

Abstract

Get full access to this article

References