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PMID: 2918540 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Stickler's syndrome.

Journal of medical genetics ·Vol. 26 ·No. 2 ·1989-02-00 ·Pages 119-26

Temple IK

Abstract

暂无摘要

MeSH Terms
Child, Preschool Diagnosis, Differential Eye Diseases/pathology Humans Infant Joint Diseases/pathology Osteochondrodysplasias/pathology Syndrome
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Temple I K
Mothercare Department of Genetics, Institute of Child Health, London.
References (20)
20 references, click to expand
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  2. HEREDITARY PROGRESSIVE ARTHRO-OPHTHALMOPATHY.
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  3. The Wagner-Stickler syndrome-a genetic study.
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  4. A dominantly inherited syndrome of hyaloideoretinal degeneration, cleft palate and maxillary hypoplasia (Cervenka syndrome).
    Birth Defects Orig Artic Ser. 1971 Jun;7(7):83-6 PMID: 5173248
  5. The Stickler syndrome.
    N Engl J Med. 1972 Mar 9;286(10):546-7 PMID: 4621768
  6. A bone dysplasia with deafness.
    Br J Radiol. 1974 May;47(557):244-51 PMID: 4830146
  7. Prevalence of mitral-valve prolapse in the Stickler syndrome.
    Am J Med Genet. 1986 Jul;24(3):387-92 PMID: 3728560
  8. [Differential diagnosis between dysostosis enchondralis and chondrodystrophy].
    Z Kinderheilkd. 1952;70(6):633-40 PMID: 12995812
  9. The Marshall syndrome: report of a new family.
    J Pediatr. 1974 Jun;84(6):868-71 PMID: 4826625
  10. The Weissenbacher-Zweymüller syndrome: possible neonatal expression of the Stickler syndrome.
    Am J Med Genet. 1982 Jan;11(1):113-9 PMID: 7064999
  11. Marshall/Stickler syndrome.
    J Med Genet. 1982 Apr;19(2):139-40 PMID: 7077624
  12. Abnormal facies, myopia, and short stature.
    Arch Dis Child. 1972 Oct;47(255):787-93 PMID: 5086512
  13. Hereditary hyaloideoretinal degeneration and palatoschisis.
    Arch Ophthalmol. 1970 Feb;83(2):152-62 PMID: 5411526
  14. Autosomal recessive deafness with skeletal dysplasia and facial appearance of Marshall syndrome.
    Am J Med Genet. 1985 Jun;21(2):317-24 PMID: 4014313
  15. Generalized osseous abnormalities in the Marshall syndrome.
    Birth Defects Orig Artic Ser. 1976;12(5):299-314 PMID: 953235
  16. The Marshall and Stickler syndromes: objective rejection of lumping.
    J Med Genet. 1984 Feb;21(1):34-8 PMID: 6694183
  17. A recessively inherited chondrodystrophy.
    Birth Defects Orig Artic Ser. 1970 Oct;6(4):25-7 PMID: 5524826
  18. The Weissenbacher-Zweymüller, Stickler, and Marshall syndromes: further evidence for their identity.
    Am J Med Genet. 1983 Oct;16(2):189-99 PMID: 6650564
  19. Ectodermal dysplasia; report of kindred with ocular abnormalities and hearing defect.
    Am J Ophthalmol. 1958 Apr;45(4 Pt 2):143-56 PMID: 13520885
  20. [SIMULTANEOUS OCCURRANCE OF THE PIERRE ROBIN SYNDROME AND FETAL CHONDRODYSPLASIA].
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Article Info
Journal
Journal of medical genetics
Abbr.
J Med Genet
ISSN
0022-2593
DOI
10.1136/jmg.26.2.119
Published
1989-02-00
Pages
119-26
Language
English
Region
England
NLM ID
2985087R
PMCID
PMC1015563
Subset
IM
External Links
PubMed source DOI: 10.1136/jmg.26.2.119 PMC Full Text View journal details
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