Skip to main content
Log in

Osteogenesis imperfecta und Glaukom

Eine Fallbeschreibung

Osteogenesis imperfecta and glaucoma

A case report

  • Kasuistiken
  • Published:
Der Ophthalmologe Aims and scope Submit manuscript

Zusammenfassung

Osteogenesis imperfecta (OI) ist eine Erkrankung des Kollagenstoffwechsels. Neben Defekten in der Knochensynthese sind okuläre Manifestationen bekannt wie blaue Skleren, Myopie, Glaukom und Keratokonus. Wir berichten über einen Patienten mit OI, bei dem bei progredienter glaukomatöser Optikusatrophie unter medikamentöser Druckregulation eine Trabekulektomie an beiden Augen durchgeführt wurde. Ein Jahr postoperativ wurde ein Augeninnendruck von 7–11 mmHg gemessen. Dieser Fallbericht zeigt exemplarisch die Besonderheiten bei fistulierender Glaukomchirurgie bei Patienten mit OI.

Abstract

Osteogenesis imperfecta (OI) is a connective tissue metabolic disorder with autosomal inheritance. Ocular involvement includes blue sclera, myopia, glaucoma and keratoconus in addition to bone synthesis defects. We report the case of a male patient with OI who suffered from progressive visual field defects and advanced glaucomatous optic atrophy and underwent trabeculectomy on both eyes. Intraocular pressures (IOP) of 7–11 mmHg were measured 1 year postoperatively. This report illustrates peculiarities in the surgical therapy of open angle glaucoma in patients with OI as well as the options for complication management.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Abb. 1
Abb. 2
Abb. 3
Abb. 4
Abb. 5

Literatur

  1. Beckh U, Schönherr U, Naumann G (1995) Autosomal dominanter Keratokonus als okuläres Leitsymptom bei Osteogenesis tarda Lobstein. Klin Monatsbl Augenheilkd 206:268–272

    Article  PubMed  CAS  Google Scholar 

  2. Byers PH, Steiner RD (1992) Osteogenesis imperfecta. Annu Rev Inc 43:269–282

    CAS  Google Scholar 

  3. Chan CC, Green WR, de la Cruz ZC, Hillis A (1982) Ocular findings in osteogenesis imperfecta congenita. Arch Ophthalmol 100:1458–1463

    Article  PubMed  CAS  Google Scholar 

  4. Chu ML, Williams CJ, Pepe G et al (1983) Internal deletion in a collagen gene in a perinatal lethal form of osteogenesis imperfecta. Nature 304:78–80

    Article  PubMed  CAS  Google Scholar 

  5. Evereklioglu C, Madenci E, Bayazit YA et al (2002) Central corneal thickness is lower in osteogenesis imperfecta and negatively correlates with the presence of blue sclera. Ophthalmic Physiol Opt 22:511–515

    Article  PubMed  Google Scholar 

  6. Forlino A, Cabral WA, Barnes AM, Marini JC (2011) New perspectives on osteogenesis imperfecta. Nat Rev Endocrinol 7(9):540–557

    Article  PubMed  CAS  Google Scholar 

  7. Rodriguez-Ares MT, Tourino R, Capeans C et al (1999) Repair of scleral perforation with preserved sceral and amniotic membrane in Marfan’s syndrome. Ophthalmic Surg Lasers 30:485–487

    PubMed  CAS  Google Scholar 

  8. Mietz H, Kasner L, Green WR (1997) Histophathological and electron-microscopic features of corneal and scleral collagen fibers in osteogenesis imperfecta typ III. Graefes Arch Clin Exp Ophthalmol 235:405–410

    Article  PubMed  CAS  Google Scholar 

  9. Zeitlin L, Fassier F, Glorieux FH (2003) Modern approach to children with osteogenesis imperfecta. J Pediatr Orthop B 12:77–87

    Article  PubMed  Google Scholar 

Download references

Interessenkonflikt

Der korrespondierende Autor gibt an, dass kein Interessenkonflikt besteht.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to H. Thieme.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Rosbach, J., Vossmerbaeumer, U., Renieri, G. et al. Osteogenesis imperfecta und Glaukom. Ophthalmologe 109, 479–482 (2012). https://doi.org/10.1007/s00347-011-2455-1

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00347-011-2455-1

Schlüsselwörter

Keywords

Navigation