Access the full text.
Sign up today, get DeepDyve free for 14 days.
R. Lowry, R. MacLean, D. McLean, B. Tischler (1971)
Cataracts, microcephaly, kyphosis, and limited joint movement in two siblings: a new syndrome.The Journal of pediatrics, 79 2
R. Wynne‐Davies, G. Lloyd-Roberts (1976)
Arthrogryposis multiplex congenita. Search for prenatal factors in 66 sporadic cases.Archives of Disease in Childhood, 51
B. Banker, M. Victor, R. Adams (1957)
Arthrogryposis multiplex due to congenital muscular dystrophy.Brain : a journal of neurology, 80 3
Sérgio Pena, M.H.K. Shokeir (1974)
Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia: a lethal condition.The Journal of pediatrics, 85 3
A. Rosenmann, I. Arad (1974)
Arthrogryposis Multiplex Congenita: Neurogenic Type with Autosomal Recessive InheritanceJournal of Medical Genetics, 11
D. Mcalpine, C. Lumsden, E. Acheson (1972)
Multiple sclerosis,: A reappraisal
Jago RH (1970)
Arthrogryposis muliplex congenita following treatment of maternal tetanus with muscle relaxantsArch Dis Child, 45
R. Jago (1970)
Arthrogryposis following treatment of maternal tetanus with muscle relaxants.Archives of Disease in Childhood, 45
Harvey FRIEDLANDER, G. Westin, WALTER Wood (1968)
Arthrogryposis Multiplex Congenita: A REVIEW OF FORTY-FIVE CASESJournal of Bone and Joint Surgery, American Volume, 50
McKusick VA (1983)
Mendelian Inheritance in Man
C. Pearson, W. Fowler (1963)
Hereditary non-progressive muscular dystrophy inducing arthrogryposis syndrome.Brain : a journal of neurology, 86
Westin GW Friedlander HL (1968)
Arthrogryposis multiplex congenita: A review of 45 casesJ Bone Joint Surg Am, 50
Daniel Drachman, AlfredJ Coulombre (1962)
Experimental clubfoot and arthrogryposis multiplex congenita.Lancet, 2 7255
D. Daentl, B. Berg, R. Layzer, C. Epstein (1974)
A new familial arthrogryposis without weaknessNeurology, 24
D. Smith (1977)
An approach to clinical dysmorphology.The Journal of pediatrics, 91 4
J. Hall, S. Reed (1982)
Teratogens associated with congenital contractures in humans and in animals.Teratology, 25 2
G. Sack (1978)
A dominantly inherited form of arthrogryposis multiplex congenita with unusual dermatoglyphicsClinical Genetics, 14
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.
Archives of Neurology – American Medical Association
Published: Nov 1, 1984
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.