» Articles » PMID: 6847514

Intrinsic Laryngeal Muscles in Oculocraniosomatic Syndrome (OCSS). An Autopsy Study

Overview
Date 1983 Jan 1
PMID 6847514
Authors
Affiliations
Soon will be listed here.
Abstract

In a 36-year-old woman who died due to an atypical subacute necrotizing inclusion-body encephalitis with herpes virions, typical clinical symptoms of the oculocraniosomatic syndrome of Kearns and Sayre were substantiated. Her still living daughter suffers from the same disorder. The skeletal muscles taken from various parts of the body of the 36-year-old patient displayed the typical features of a sudanophilic myopathy, including abundant 'ragged-red' fibers and a pleoconial mitochondriosis. For the first time in the literature the intrinsic laryngeal muscles were also found to be significantly involved. Their morphological features are delineated and discussed.

References
1.
Robertson Jr W, Viseskul C, Lee Y, Lloyd R . Basal ganglia calcification in Kearns-Sayre syndrome. Arch Neurol. 1979; 36(11):711-3. DOI: 10.1001/archneur.1979.00500470081017. View

2.
Kearns T . External Ophthalmoplegia, Pigmentary Degeneration of the Retina, and Cardiomyopathy: A Newly Recognized Syndrome. Trans Am Ophthalmol Soc. 1965; 63:559-625. PMC: 1310209. View

3.
Groothuis D, Schulman S, Wollman R, Frey J, Vick N . Demyelinating radiculopathy in the Kearns-Sayre syndrome: a clinicopathological study. Ann Neurol. 1980; 8(4):373-80. DOI: 10.1002/ana.410080406. View

4.
Schmitt H, Krause K . An autopsy study of a familial oculopharyngeal muscular dystrophy (OPMD) with distal spread and neurogenic involvement. Muscle Nerve. 1981; 4(4):296-305. DOI: 10.1002/mus.880040406. View

5.
Cohen S . Arythenoidectomy in children. Laryngoscope. 1973; 83(8):1293-9. DOI: 10.1288/00005537-197308000-00013. View