[Spontaneous rupture of the anterior lens capsule in Alport syndrome (case study)]. / Samoproizvol'noe vskrytie perednei kapsuly khrustalika pri sindrome Al'porta (klinicheskoe nablyudenie).
Vestn Oftalmol
; 140(3): 76-81, 2024.
Article
em Ru
| MEDLINE
| ID: mdl-38962982
ABSTRACT
Alport syndrome is a hereditary disease characterized by glomerulopathy, manifested by hematuria and/or proteinuria, progressive decline in renal function, often combined with hearing and vision pathology. This article presents a clinical case of spontaneous opening of the anterior lens capsule in a patient with Alport syndrome, accompanied by uveitis and ophthalmic hypertension, and describes the features of the surgical aid and the postoperative period.
Palavras-chave
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Nefrite Hereditária
Limite:
Adult
/
Humans
/
Male
Idioma:
Ru
Revista:
Vestn Oftalmol
Ano de publicação:
2024
Tipo de documento:
Article
País de afiliação:
Federação Russa