» Articles » PMID: 6650144

Lipid Storage Myopathy Associated with Scoliosis and Multiple Joint Contractures

Overview
Specialty Neurology
Date 1983 Jan 1
PMID 6650144
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Two patients with cleft palate, clubfoot, congenital scoliosis, and arthrogryposis multiplex congenita showed increased numbers of lipid droplets in biopsied muscle fibers. There was little abnormality in the mitochondrial morphology of the muscle and the results of blood chemistry including carnitine concentrations. Accumulation of large lipid droplets, increased amount of glycogen and a decreased number of mitochondria were observed in chondrocytes from the biopsied iliac crest cartilage of these patients. It was suggested that the present cases might belong to a previously unknown clinico-pathological entity of myopathies.

Citing Articles

Comparative proteomics analysis for identifying the lipid metabolism related pathways in patients with Klippel-Feil syndrome.

Li Z, Zhang C, Qiu B, Niu Y, Leng L, Cai S Ann Transl Med. 2021; 9(3):255.

PMID: 33708882 PMC: 7940892. DOI: 10.21037/atm-20-5155.


Integrated bioinformatics analysis of potential pathway biomarkers using abnormal proteins in clubfoot.

Cai G, Yang X, Chen T, Jin F, Ding J, Wu Z PeerJ. 2020; 8:e8422.

PMID: 31998564 PMC: 6977474. DOI: 10.7717/peerj.8422.


Diagnosing arthrogryposis multiplex congenita: a review.

Kalampokas E, Kalampokas T, Sofoudis C, Deligeoroglou E, Botsis D ISRN Obstet Gynecol. 2012; 2012:264918.

PMID: 23050160 PMC: 3461621. DOI: 10.5402/2012/264918.


Congenital scoliosis in a neonate: can a neonatologist ignore it?.

Jog S, Patole S, Whitehall J Postgrad Med J. 2002; 78(922):469-72.

PMID: 12185219 PMC: 1742463. DOI: 10.1136/pmj.78.922.469.


Primary lipid cardiomyopathy.

Zimmermann A, Wyss P, Stocker F Virchows Arch A Pathol Anat Histopathol. 1990; 416(5):453-9.

PMID: 2107634 DOI: 10.1007/BF01605153.

References
1.
Cornelio F, Di Donato S, Peluchetti D, Bizze A, Bertagnolio B, DAngelo A . Fatal cases of lipid storage myopathy with carnitine deficiency. J Neurol Neurosurg Psychiatry. 1977; 40(2):170-8. PMC: 492634. DOI: 10.1136/jnnp.40.2.170. View

2.
Jerusalem F, Angelini C, Engel A, GROOVER R . Mitochondria-lipid-glycogen (MLG) disease of muscle. A morphologically regressive congenital myopathy. Arch Neurol. 1973; 29(3):162-9. DOI: 10.1001/archneur.1973.00490270044007. View

3.
Cederblad G, Lindstedt S . A method for the determination of carnitine in the picomole range. Clin Chim Acta. 1972; 37:235-43. DOI: 10.1016/0009-8981(72)90438-x. View

4.
BOUDIN G, Mikol J, Guillard A, Engel A . Fatal systemic carnitine deficiency with lipid storage in skeletal muscle, heart, liver and kidney. J Neurol Sci. 1976; 30(2-3):313-25. DOI: 10.1016/0022-510x(76)90137-4. View

5.
Engel A, Angelini C . Carnitine deficiency of human skeletal muscle with associated lipid storage myopathy: a new syndrome. Science. 1973; 179(4076):899-902. DOI: 10.1126/science.179.4076.899. View