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Biomedical subjects

Eva Wolter-Roessler

Publications and source records attributed to Eva Wolter-Roessler.

2 recordsLinked to original sources

[Amblyopia of the fellow eye in assumed unilateral congenital fibrosis syndrome].

BACKGROUND: Amblyopia of the ptotic eye in spite of head posturing and of the fellow eye in ptosis with motility disorders are well known. We emphasize the importance of exact ophthalmological and orthoptic examinations to avoid amblyopia in both ptosis and fellow eye, even in cases of mild ptosis, especially if they are combined with motility disorders. PATIENT: A 5 year-old girl presented to our outpatient clinic because of ptosis of the left eye and hypertropia of the right eye. Visual acuity of the right eye was 0.32 and of the left ptotic eye 1.0. Cycloplegic retinoscopy showed + 2.0 sphere in both eyes. Ocular motility showed a mild reduction of elevation of the left eye in ad- and abduction. This led to the diagnosis of congenital fibrosis syndrome of the inferior rectus muscle of the left eye. Due to the preferred fixation with the left ptotic eye and the consecutive deviation of the fellow eye amblyopia of the right eye had developed. Occlusion therapy of the left eye resulted in an improvement of visual acuity of the right eye to 0.9 and centralisation of fixation within one month. CONCLUSION: Even children with mild ptosis, especially in combination with motility disorders, require a complete ophthalmological and orthoptic examination to avoid amblyopia also of the fellow eye.

Blepharoptosis↗

[Pterygoid corneal dystrophy].

BACKGROUND: Pterygia are characterised by progressive growth of fibrovascular tissue over the nasal limbus towards the corneal center with the loss of Bowman's layer. We report on three patients with bilateral symmetrical affection of the nasal and temporal limbus in one family. PATIENTS: A 81-year-old female, her 61-year-old son and her 37-year-old grandson presented with a familiar form of pterygium-like corneal changes. Remarkable was the bilateral symmetrical affection with involvement of the nasal and temporal limbus. Both male patients had multiple excisions (including lamellar keratoplasty) but suffered from persistent recurrences, which led to sustained reduction of the visual acuity. Histological examination revealed typical elastoid degeneration of collagen fibres. CONCLUSION: We assume autosomal dominant heredity with varying expression for this "pterygoid corneal dystrophy". It does not seem to differ histologically from normal pterygia, but recurrences appear to be more frequent and more aggressive.

Adult↗