Objective: To describe the recurrence of a chemical burn injury in three half-siblings. Methodology: This is a descriptive study of the case report of three half-siblings with blindness. Description: The case presented regards three half-siblings aging 13 years old, 3 years old and 17 months who presented blindness with characteristics compatible with chemical ocular injury. Comments: It is estimated that 14 million of the world's children are blind and the impact of this problem is significantly negative. The chemical burn is one of many causes of child blindness, and sometimes it is triggered by aggression. Munchausen's Syndrome by proxy is a form of abuse in which the female genitor/offender invents or causes illness in the victim. The d...
Background: .To study the causes of visual disability and severity of blindness in blind school chil...
CONTEXT: Leber's hereditary optic neuropathy is an important cause of progressive painless visual lo...
PURPOSE: To report a novel presentation of dyskeratosis congenita masquerading as familial exudative...
Objective: To present a scourge of blindness possibly due to an inherited condition causing retinal ...
Objective: To present a scourge of blindness possibly due to an inherited condition causing retinal ...
Background/Purpose: To review the pattern of presentation and management difficulty of patients wit...
Purpose: To describe a previously unreported condition involving familial spastic paraplegia and a p...
AIM:To analyze the pathogenesis, refraction states, refractive error correction with glasses and dis...
Purpose: We report a rare case of CRB1 gene mutation in two siblings (sisters) affected with the exa...
Two siblings were referred for workup for progres-sive neurological deterioration. The elder sibling...
Contains fulltext : 59228.pdf (publisher's version ) (Closed access)OBJECTIVE: To ...
Purpose: To study long-term outcome of SBS on visual and cognitive functions. Methods: Case series ...
Purpose: Strabismus, a manifest misalignment of the visual axes, is one of the most common childhood...
PURPOSE: To report the clinical features and outcome of a series of children with optic neuritis. ME...
PURPOSE: To report the ophthalmologic characteristics of a newly identified seven generation pedigre...
Background: .To study the causes of visual disability and severity of blindness in blind school chil...
CONTEXT: Leber's hereditary optic neuropathy is an important cause of progressive painless visual lo...
PURPOSE: To report a novel presentation of dyskeratosis congenita masquerading as familial exudative...
Objective: To present a scourge of blindness possibly due to an inherited condition causing retinal ...
Objective: To present a scourge of blindness possibly due to an inherited condition causing retinal ...
Background/Purpose: To review the pattern of presentation and management difficulty of patients wit...
Purpose: To describe a previously unreported condition involving familial spastic paraplegia and a p...
AIM:To analyze the pathogenesis, refraction states, refractive error correction with glasses and dis...
Purpose: We report a rare case of CRB1 gene mutation in two siblings (sisters) affected with the exa...
Two siblings were referred for workup for progres-sive neurological deterioration. The elder sibling...
Contains fulltext : 59228.pdf (publisher's version ) (Closed access)OBJECTIVE: To ...
Purpose: To study long-term outcome of SBS on visual and cognitive functions. Methods: Case series ...
Purpose: Strabismus, a manifest misalignment of the visual axes, is one of the most common childhood...
PURPOSE: To report the clinical features and outcome of a series of children with optic neuritis. ME...
PURPOSE: To report the ophthalmologic characteristics of a newly identified seven generation pedigre...
Background: .To study the causes of visual disability and severity of blindness in blind school chil...
CONTEXT: Leber's hereditary optic neuropathy is an important cause of progressive painless visual lo...
PURPOSE: To report a novel presentation of dyskeratosis congenita masquerading as familial exudative...