Trichothiodystrophy: a case report of childhood glaucoma associated with non-acquired systemic disease

Trichothiodystrophy belongs to a group of rare genetic diseases characterized by DNA repair anomalies. Ocular manifestations can occur in 50% of cases, including cataract, refractive errors, strabismus, microcornea, microphthalmia, dry eye, and pigmentary macular changes. We report a case of childho...

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Veröffentlicht in:Arquivos brasileiros de oftalmologia 2018, Vol.81 (6), p.520-523
Hauptverfasser: Silva, Diana Silveira, Almeida, Izabela, Netto, Camila F, Esporcatte, Bruno L B, Rolim-de-Moura, Christiane
Format: Report
Sprache:eng
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Zusammenfassung:Trichothiodystrophy belongs to a group of rare genetic diseases characterized by DNA repair anomalies. Ocular manifestations can occur in 50% of cases, including cataract, refractive errors, strabismus, microcornea, microphthalmia, dry eye, and pigmentary macular changes. We report a case of childhood glaucoma in a patient with trichothiodystrophy who underwent trabeculectomy in the left eye. To our knowledge, this is the first clinical report of childhood glaucoma associated with trichothiodystrophy.
ISSN:1678-2925
DOI:10.5935/0004-2749.20180101