1. Congenital keratoglobus with blue sclera in two siblings with overlapping Marshall/Stickler phenotype.
- Author
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Imamoglu S, Kaya V, Imamoglu EY, and Gok K
- Subjects
- Child, Child, Preschool, Corneal Topography, Female, Humans, Phenotype, Visual Acuity, Abnormalities, Multiple, Cataract diagnosis, Collagen Type XI deficiency, Cornea abnormalities, Craniofacial Abnormalities diagnosis, Eye Diseases, Hereditary diagnosis, Genetic Diseases, X-Linked diagnosis, Hearing Loss, Sensorineural diagnosis, Osteochondrodysplasias diagnosis, Sclera abnormalities, Siblings
- Abstract
We aimed to describe congenital keratoglobus with blue sclera in two siblings with overlapping Marshall/Stickler phenotype. Two sisters (ages four and six) with bilateral high astigmatism were evaluated by slit-lamp microscopy. Corneal topography and pachymetry maps were also obtained. Slit-lamp examination revealed that both corneas were globular in shape with peripheral corneal thinning. Pachymetry maps showed diffuse corneal thinning. Two siblings had in common the features of keratoglobus, blue sclera, atypical face, hearing loss, and hypermobile joints. We tentatively diagnosed the sisters as having an overlapping Marshall-Stickler phenotype based on clinical and radiological findings. Marshall-Stickler syndrome may exist in the differential diagnosis of keratoglobus with blue sclera., Competing Interests: There are no conflicts of interest.
- Published
- 2016
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