2012, Number 4
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Rev Méd Electrón 2012; 34 (4)
Anomaly of Axenfeld-Rieger: presentation of a case
Armengol OY, de Armas HN, Alemán SIO, Suárez HV
Language: Spanish
References: 12
Page: 483-489
PDF size: 401.78 Kb.
ABSTRACT
We made the clinical presentation of a female patient who assisted the ophthalmologic consultation to follow her by glaucoma and was diagnosed with an Axenfeld-Rieger anomaly for presenting, in a bilateral and asymmetric way. the alterations in the anterior segment of the eye that are typical of this rare ocular disease such as: a prominent Schwalbe ring displaced forward, irido-corneal adherences, and stromatic atrophy of the iris. This anomaly belongs to the group of the so called irido-corneal dysgenics that generally develops with a secondary ocular hypertension, being that the feature of its importance from the ophthalmologic point of view. The ocular tension of the patients has been kept under control with medical treatment.
REFERENCES
Ayala Barroso E, Alvarez Marín J, Delgado Miranda Jl. Síndrome de Axenfeld-Rieger. Arch Soc Canar Oftal [Internet]. 1999 [citado 6 Jun 2011];(10). Disponible en: http://www.oftalmo.com/sco/revista-10/sco17.htm.
Roldán Valdés DM. Anomalía de Rieger: reporte de una familia. An Soc Mex Oftalmol [Internet]. 1986 [citado 6 Jun 2012];60(1):29-35. Disponible en: http://bases.bireme.br/cgi-bin/wxislind.exe/iah/online/?IsisScript=iah/iah.xis&src=google&base=ADOLEC&lang=p&nextAction=lnk&exprSearch=47057&indexSearch=ID.
Avellaneda A, Izquierdo AM. Síndrome de Axenfeld Riger. Instituto de Investigación de enfermedades raras. Código CIE-9-MC; 2004. p. 743-44.
Walter MA, Mirzayans F, Mears AJ. Autosomal-dominant iridogoniodysgenesis and Axenfeld-Rieger syndrome are genetically distinct. Ophthalmology [Internet]. 2006 [citado 7 Jun 2011];103(11):1907-15. Disponible en: http://www.ncbi.nlm.nih.gov/pubmed/8942889.
Flores Pérez D, Labrada Rodríguez YH, González Leyva M. Síndrome Axenfeld-Rieger. Presentación de un caso. Rev Cubana Oftalmol [Internet]. 2000 [citado 7 Jun 2011];13(1):16-9. Disponible en: http://scielo.sld.cu/scielo.php?script=sci_arttext&pid=S0864-21762000000100003&lng=es&nrm=iso&tlng=es.
Eguia Martínez F, Río Torres M, Capote Cabrera A. Manual de diagnóstico y tratamiento en Oftalmología. La Habana: Editorial Ciencias Médicas; 2009 [citado 7 Jun 2011]. Disponible en: http://www.bvs.sld.cu/libros/manual_diag_ttmo_oftalmologia/indice_p.htm.
Vaughan D, Asbury T. General Ophthalmology. Glaucoma. 17th ed. New York: McGraw-Hill Companies; 2008.
Peñate Santana H, García González M. Crisis de hipertensión ocular en el Síndrome de Rieger: a propósito de un caso. Arch Soc Canar Octal [Internet]. 2010 [citado 7 Jun 2011];(21). Disponible en: http://www.oftalmo.com/sco/revista-21/21sco10.htm.
Spierer A, Barak A. Anterior segment pathology associated with hypermetropia. Ophthalmic Genetics [Internet]. 1996 [citado 7 Jun 2011];17(2):79-83. Disponible en: http://informahealthcare.com/doi/abs/10.3109/13816819609057875.
Cella W, Cabral De Vasconcellos JP, Barbosa De Melo M, Kneipp B, Ferreira Costa F, Longui CA, et al. Structural assessment of PITX2, FOXC1, CYP1B1, and GJA1 genes in patients with Axenfeld-Rieger syndrome with developmental glaucoma. Invest Ophthalmol Vis Sci [Internte]. 2006 May [citado 7 Jun 2011];47(5):1803-09. Disponible en: http://www.iovs.org/content/47/5/1803.short.
American Academy of Oftalmology. Glaucoma. USA: American Academy of Oftalmology; 2008.
Dressler P, Gramer E. Morphology, family history, and age at diagnosis of 26 patients with Axenfeld-Rieger syndrome and glaucoma or ocular hypertension. Ophthalmologe. 2006 May;103(5):393-400. Citado en Pubmed; PMID: 16683168.