Barceló Mendiguchia, Ana Gutiérrez Díaz, Esperanza Sánchez del Pozo, Jaime Tejada Palacios, Pilar
Glaucoma hereditario asociado a displasia oculodentodigital [artículo] - Archivos de la Sociedad Española de Oftalmología, 2011 - 86(9):292-294.
Formato Vancouver:
Tejada P, Eduardo YW, Gutiérrez E, Barceló A, Sánchez J. Glaucoma hereditario asociado a displasia oculodentodigital. Arch Soc Esp Oftalmol. 2011;86(9):292-4.
PMID: 21893263
Contiene 4 referencias
CASE REPORT: A newborn evaluated at 20 days old due to occasional nystagmus. Her mother had presented with oculodentodigital dysplasia (ODDD) and glaucoma. The physical examination revealed opaque micro-corneas, and horizontal nystagmus. The tonometry showed 35 mm Hg in OD and 40 mm Hg in OS and the fundus examination was normal. She had a narrow nasal bridge with narrow nostrils, and fourth and fifth finger syndactylyl in both hands. A bilateral trabeculectomy was performed with a good response. DISCUSSION: ODDD is a rare autosomal dominant disease with heterogeneous phenotype manifestations. The most frequent cause of loss of visual acuity is the glaucoma, requiring long-term follow up with periodical control of the intraocular pressure (IOP).
Glaucoma hereditario asociado a displasia oculodentodigital [artículo] - Archivos de la Sociedad Española de Oftalmología, 2011 - 86(9):292-294.
Formato Vancouver:
Tejada P, Eduardo YW, Gutiérrez E, Barceló A, Sánchez J. Glaucoma hereditario asociado a displasia oculodentodigital. Arch Soc Esp Oftalmol. 2011;86(9):292-4.
PMID: 21893263
Contiene 4 referencias
CASE REPORT: A newborn evaluated at 20 days old due to occasional nystagmus. Her mother had presented with oculodentodigital dysplasia (ODDD) and glaucoma. The physical examination revealed opaque micro-corneas, and horizontal nystagmus. The tonometry showed 35 mm Hg in OD and 40 mm Hg in OS and the fundus examination was normal. She had a narrow nasal bridge with narrow nostrils, and fourth and fifth finger syndactylyl in both hands. A bilateral trabeculectomy was performed with a good response. DISCUSSION: ODDD is a rare autosomal dominant disease with heterogeneous phenotype manifestations. The most frequent cause of loss of visual acuity is the glaucoma, requiring long-term follow up with periodical control of the intraocular pressure (IOP).
