Literature DB >> 11388760

Clinical features of hereditary progressive arthro-ophthalmopathy (Stickler syndrome): a survey.

G B Stickler1, W Hughes, P Houchin.   

Abstract

PURPOSE: To define variations in the clinical manifestations of Stickler syndrome.
METHODS: A questionnaire was sent to 612 persons.
RESULTS: Of the 316 usable replies, 95% of persons had eye problems (retinal detachment occurred in 60% of patients, myopia in 90%, and blindness in 4%); 84% had problems with facial structures such as a flat face, small mandible, or cleft palate; 70%, hearing loss; and 90%, joint problems, primarily early joint pain from degenerative joint disease. Treatment included cryotherapy and laser therapy for retinal detachment, repair of cleft palate, use of hearing and mobility aids, and joint replacements.
CONCLUSIONS: There are wide variations of symptoms and signs among affected persons, even within the same family. There are delays in diagnosis, lack of understanding among family members, denial about the risk of serious eye problems, and joint disease.

Entities:  

Mesh:

Year:  2001        PMID: 11388760     DOI: 10.1097/00125817-200105000-00008

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  40 in total

1.  Stickler syndrome caused by COL2A1 mutations: genotype-phenotype correlation in a series of 100 patients.

Authors:  Kristien P Hoornaert; Inge Vereecke; Chantal Dewinter; Thomas Rosenberg; Frits A Beemer; Jules G Leroy; Laila Bendix; Erik Björck; Maryse Bonduelle; Odile Boute; Valerie Cormier-Daire; Christine De Die-Smulders; Anne Dieux-Coeslier; Hélène Dollfus; Mariet Elting; Andrew Green; Veronica I Guerci; Raoul C M Hennekam; Yvonne Hilhorts-Hofstee; Muriel Holder; Carel Hoyng; Kristi J Jones; Dragana Josifova; Ilkka Kaitila; Suzanne Kjaergaard; Yolande H Kroes; Kristina Lagerstedt; Melissa Lees; Martine Lemerrer; Cinzia Magnani; Carlo Marcelis; Loreto Martorell; Michèle Mathieu; Meriel McEntagart; Angela Mendicino; Jenny Morton; Gabrielli Orazio; Véronique Paquis; Orit Reish; Kalle O J Simola; Sarah F Smithson; Karen I Temple; Elisabeth Van Aken; Yolande Van Bever; Jenneke van den Ende; Johanna M Van Hagen; Leopoldo Zelante; Riina Zordania; Anne De Paepe; Bart P Leroy; Marc De Buyzere; Paul J Coucke; Geert R Mortier
Journal:  Eur J Hum Genet       Date:  2010-02-24       Impact factor: 4.246

Review 2.  A role for epigenetics in hearing: Establishment and maintenance of auditory specific gene expression patterns.

Authors:  Matthew J Provenzano; Frederick E Domann
Journal:  Hear Res       Date:  2007-07-19       Impact factor: 3.208

Review 3.  Syndromic Hearing Loss: A Brief Review of Common Presentations and Genetics.

Authors:  John D Gettelfinger; John P Dahl
Journal:  J Pediatr Genet       Date:  2018-01-04

Review 4.  Stickler syndrome, ocular-only variants and a key diagnostic role for the ophthalmologist.

Authors:  M P Snead; A M McNinch; A V Poulson; P Bearcroft; B Silverman; P Gomersall; V Parfect; A J Richards
Journal:  Eye (Lond)       Date:  2011-09-16       Impact factor: 3.775

5.  Adult presentation of Stickler syndrome type III.

Authors:  Kayi Li; Carter Thorne
Journal:  Clin Rheumatol       Date:  2010-01-30       Impact factor: 2.980

6.  Outcomes of surgery for retinal detachment in patients with Stickler syndrome: a comparison of two sequential 20-year cohorts.

Authors:  Poorna Abeysiri; Catey Bunce; Lyndon da Cruz
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2007-06-20       Impact factor: 3.117

7.  [Retinal detachment in pediatrics : Etiology and risk factors].

Authors:  C Bier; A Kampik; A Gandorfer; O Ehrt; G Rudolph
Journal:  Ophthalmologe       Date:  2010-02       Impact factor: 1.059

8.  Osteochondritis dissecans and Osgood Schlatter disease in a family with Stickler syndrome.

Authors:  Ali Al Kaissi; Klaus Klaushofer; Franz Grill
Journal:  Pediatr Rheumatol Online J       Date:  2009-02-04       Impact factor: 3.054

Review 9.  Recent developments in our understanding of how platelet-derived growth factor (PDGF) and its receptors contribute to proliferative vitreoretinopathy.

Authors:  Hetian Lei; Marc-Andre Rheaume; Andrius Kazlauskas
Journal:  Exp Eye Res       Date:  2009-11-25       Impact factor: 3.467

Review 10.  Arachnodactyly--a key to diagnosing heritable disorders of connective tissue.

Authors:  Rodney Grahame; Alan J Hakim
Journal:  Nat Rev Rheumatol       Date:  2013-03-12       Impact factor: 20.543

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