The hip in Stickler syndrome

Journal of Pediatric Orthopaedics

Volumn 21, Issue 5, 2001, Pages 657-663

  Rose, Peter S ^a,b,d   Ahn, Nicholas U ^b   Levy, Howard P ^a,c   Magid, Donna ^b,c   Davis, Joie ^a   Liberfarb, Ruth M ^a   Sponseller, Paul D ^b   Francomano, Clair A ^a  

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^b JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c JOHNS HOPKINS HOSPITAL   (United States)

^d MAYO CLINIC   (United States)

Author keywords

Hereditary arthro ophthalmopathy; Legg Perthes disease; Osteoarthritis; Protrusio acetabuli; Slipped epiphysis; Stickler syndrome

Indexed keywords

ADOLESCENT; ADULT; AGING; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHILD; CONNECTIVE TISSUE DISEASE; CORRELATION FUNCTION; FEMALE; HIP DISEASE; HUMAN; MAJOR CLINICAL STUDY; MALE; OSTEOARTHRITIS; PAIN; PRIORITY JOURNAL; STICKLER SYNDROME;

ABNORMALITIES, MULTIPLE; ADULT; AGE DISTRIBUTION; BONE DISEASES, DEVELOPMENTAL; CONNECTIVE TISSUE DISEASES; FEMALE; HEARING LOSS, SENSORINEURAL; HIP JOINT; HUMANS; MALE; OSTEOARTHRITIS, HIP; PAIN; RETINAL DISEASES; SYNDROME;

EID: 0034875757     PISSN: 02716798     EISSN: None     Source Type: Journal    
DOI: 10.1097/00004694-200109000-00020     Document Type: Article

References (48)

1. A second mutation in the type II procollagen gene (COL2AI) causing stickler syndrome (arthro-ophthalmopathy) is also a premature termination codon
2. The adult hip: An anatomic study. Part I: The bony landmarks
3. The epidemiology of Perthes' disease
4. Hereditary arthro-ophthalmopathy (the Stickler syndrome). Report of a kindred with protrusio acetabuli
5. Stickler syndrome
6. Disorders of collagen biosynthesis and structure
7. Intraarticular lipoma in Stickler syndrome
8. Development of the Wisconsin Brief Pain Questionnaire to assess pain in cancer and other diseases
9. The Stickler syndrome: Evidence for close linkage to the structural gene for type II collagen
10. Evaluation of the measurement methods for protrusio acetabuli in normal children
11. The Stickler syndrome (hereditary arthroophthalmopathy)
12. The incidence of physiolysis of the hip: A population-based study of 175 patients
13. Normal axial relationships of the major joints
14. Radiologic assessment of osteoarthritis
15. Genetic linkage analysis of hereditary arthro-ophthalmopathy (Stickler syndrome) and the type II procollagen gene
16. Radiographic indices for osteoarthritis
17. The spinal manifestations of Stickler's syndrome
18. The arthropathy of hereditary arthroophthalmopathy (Stickler syndrome)
19. The Wagner-Stickler syndrome
20. The Wagner-Stickler syndrome: A genetic study
21. The Wagner-Stickler syndrome: A study of 22 families
22. Stickler syndrome: Further mutations in COL11A1 and evidence for additional locus heterogeneity
23. Stickler's syndrome
24. Online Mendelian inheritance in man
25. Online Mendelian inheritance in man
26. The Stickler syndrome
27. Stickler's syndrome (hereditary progressive arthro-ophthalmopathy)
28. Hereditary arthro-ophthalmopathy (Stickler syndrome): A diagnosis to consider in familial premature osteoarthritis
29. Thoracolumbar spinal abnormalities in Stickler syndrome
30. Incidence and severity of pain in Stickler and Ehlers-Danlos syndromes
31. Proposed diagnostic criteria for Stickler syndrome
32. The Stickler syndrome (hereditary arthro-ophthalmopathy)
33. Stickler syndrome without eye involvement is caused by mutations in COL11A2, the gene encoding the alpha2(XI) chain of type XI collagen
34. Clinical and molecular genetics of Stickler syndrome
35. Stickler syndrome type 2 and linkage to the COL11A1 gene
36. Stickler's syndrome: A study of 12 families
37. The epiphyseal dysplasias
38. Hereditary progressive arthro-ophthalmopathy
39. Hereditary progressive arthro-ophthalmopathy II: Additional observations on vertebral abnormalities, a hearing defect, and a report of a similar case
40. Factors associated with hip osteoarthritis: Data from the First National Health and Nutrition Examination Survey (NHANES-I)
41. Radiographic evaluation of the hip
42. Osteochondritis dissecans of the knee in an adult with Stickler syndrome
43. Otospondylomegaepiphyseal dysplasia (OSMED): Clinical description of three patients homozygous for a missense mutation in the COL11A2 gene
44. Ocular and systemic manifestations of Stickler's syndrome: A preliminary report
45. A-2→G transition at the 3′ acceptor splice site of IVS17 characterizes the COL2A1 gene mutation in the original Stickler syndrome kindred
46. Prenatal exclusion of Stickler syndrome
47. Variability of Stickler syndrome