Get 20M+ Full-Text Papers For Less Than $1.50/day. Start a 14-Day Trial for You or Your Team.

Learn More →

Arthrogryposis Multiplex Congenita Occurring With Maternal Multiple Sclerosis

Arthrogryposis Multiplex Congenita Occurring With Maternal Multiple Sclerosis Abstract • All children of a mother with multiple sclerosis (MS) had increasing grades of congenital joint contractures without demonstrable neuromuscular disease. Two had talipes equinovarus, one had congenital hip subluxation, and the youngest had arthrogryposis multiplex congenita. Maternal MS may be causally related to the development of congenital joint contractures. References 1. Banker BQ, Victor M, Adams RD: Arthrogryposis multiplex due to congenital muscular dystrophy . Brain 1957;80:319-334.Crossref 2. Daentl DL, Berg BO, Layzer RB, et al: A new familial arthrogryposis without weakness . Neurology 1974;24:55-60.Crossref 3. Rosenmann A, Arad I: Arthrogryposis multiplex congenita: Neurogenic type with autosomal recessive inheritance . J Med Genet 1974; 11:91-94.Crossref 4. McKusick VA: Mendelian Inheritance in Man , ed 6. Baltimore, Johns Hopkins University Press, 1983. 5. Smith DW: An approach to clinical dysmorphology . J Pediatr 1977;91:690-692.Crossref 6. Hall JG, Reed SD: Teratogens associated with congenital contractures in humans and in animals . Teratology 1982;25:173-191.Crossref 7. Wynne-Davies R, Lloyd-Roberts GC: Arthrogryposis multiplex congenita: Search for prenatal factors in 66 sporadic cases . Arch Dis Child 1976;51:618-623.Crossref 8. Friedlander HL, Westin GW, Wood WL: Arthrogryposis multiplex congenita: A review of 45 cases . J Bone Joint Surg Am 1968;50:89-112. 9. Pearson CM, Fowler WM Jr: Hereditary non-progressive muscular dystrophy including arthrogryposis syndrome . Brain 1963;86:75-88.Crossref 10. Pena SDJ, Shokeir MHK: Syndrome of camptodactyly, multiple ankyloses, facial anomalies and pulmonary hypoplasia: A lethal condition . J Pediatr 1974;85:373-375.Crossref 11. Lowry RB, MacLean R, McLean DM, et al: Cataracts, microcephaly, kyphosis, and limited joint movement in two siblings: A new syndrome . J Pediatr 1971;79:282-284.Crossref 12. Sack GH Jr: A dominantly inherited form of arthrogryposis multiplex congenita with unusual dermatoglyphics . Clin Genet 1978; 14:317-323.Crossref 13. Drachman DB, Coulombre AJ: Experimental clubfoot and arthrogryposis multiplex congenita . Lancet 1962;2:523-526.Crossref 14. Jago RH: Arthrogryposis muliplex congenita following treatment of maternal tetanus with muscle relaxants . Arch Dis Child 1970;45:277-279.Crossref 15. McAlpine D, Lumsden CE, Archeson ED: Multiple Sclerosis: A Reappraisal ed 2. New York, Churchill Livingstone, 1972, pp 107-109. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Archives of Neurology American Medical Association

Arthrogryposis Multiplex Congenita Occurring With Maternal Multiple Sclerosis

Archives of Neurology , Volume 41 (11) – Nov 1, 1984

Loading next page...
 
/lp/american-medical-association/arthrogryposis-multiplex-congenita-occurring-with-maternal-multiple-sz8uaS0PAd

References (17)

Publisher
American Medical Association
Copyright
Copyright © 1984 American Medical Association. All Rights Reserved.
ISSN
0003-9942
eISSN
1538-3687
DOI
10.1001/archneur.1984.04050220118031
Publisher site
See Article on Publisher Site

Abstract

Abstract • All children of a mother with multiple sclerosis (MS) had increasing grades of congenital joint contractures without demonstrable neuromuscular disease. Two had talipes equinovarus, one had congenital hip subluxation, and the youngest had arthrogryposis multiplex congenita. Maternal MS may be causally related to the development of congenital joint contractures. References 1. Banker BQ, Victor M, Adams RD: Arthrogryposis multiplex due to congenital muscular dystrophy . Brain 1957;80:319-334.Crossref 2. Daentl DL, Berg BO, Layzer RB, et al: A new familial arthrogryposis without weakness . Neurology 1974;24:55-60.Crossref 3. Rosenmann A, Arad I: Arthrogryposis multiplex congenita: Neurogenic type with autosomal recessive inheritance . J Med Genet 1974; 11:91-94.Crossref 4. McKusick VA: Mendelian Inheritance in Man , ed 6. Baltimore, Johns Hopkins University Press, 1983. 5. Smith DW: An approach to clinical dysmorphology . J Pediatr 1977;91:690-692.Crossref 6. Hall JG, Reed SD: Teratogens associated with congenital contractures in humans and in animals . Teratology 1982;25:173-191.Crossref 7. Wynne-Davies R, Lloyd-Roberts GC: Arthrogryposis multiplex congenita: Search for prenatal factors in 66 sporadic cases . Arch Dis Child 1976;51:618-623.Crossref 8. Friedlander HL, Westin GW, Wood WL: Arthrogryposis multiplex congenita: A review of 45 cases . J Bone Joint Surg Am 1968;50:89-112. 9. Pearson CM, Fowler WM Jr: Hereditary non-progressive muscular dystrophy including arthrogryposis syndrome . Brain 1963;86:75-88.Crossref 10. Pena SDJ, Shokeir MHK: Syndrome of camptodactyly, multiple ankyloses, facial anomalies and pulmonary hypoplasia: A lethal condition . J Pediatr 1974;85:373-375.Crossref 11. Lowry RB, MacLean R, McLean DM, et al: Cataracts, microcephaly, kyphosis, and limited joint movement in two siblings: A new syndrome . J Pediatr 1971;79:282-284.Crossref 12. Sack GH Jr: A dominantly inherited form of arthrogryposis multiplex congenita with unusual dermatoglyphics . Clin Genet 1978; 14:317-323.Crossref 13. Drachman DB, Coulombre AJ: Experimental clubfoot and arthrogryposis multiplex congenita . Lancet 1962;2:523-526.Crossref 14. Jago RH: Arthrogryposis muliplex congenita following treatment of maternal tetanus with muscle relaxants . Arch Dis Child 1970;45:277-279.Crossref 15. McAlpine D, Lumsden CE, Archeson ED: Multiple Sclerosis: A Reappraisal ed 2. New York, Churchill Livingstone, 1972, pp 107-109.

Journal

Archives of NeurologyAmerican Medical Association

Published: Nov 1, 1984

There are no references for this article.