Congenital sensory neuropathy. Ophthalmological implications

• Published in: Acta ophthalmologica Vol. 66; no. 3; p. 293
• Main Authors: Pinckers, A, van 't Pad Bosch, A A, Aandekerk, A L, Cruysberg, J R
• Format: Journal Article
• Language: English
• Published: Denmark 01.06.1988
• Subjects: Adult; Conjunctival Diseases - congenital; Conjunctival Diseases - etiology; Contact Lenses, Hydrophilic; Corneal Diseases - congenital; Corneal Diseases - etiology; Corneal Diseases - therapy; Female; Hereditary Sensory and Autonomic Neuropathies - complications; Humans; Keratitis, Herpetic - complications
• ISSN: 0001-639X
• DOI: 10.1111/j.1755-3768.1988.tb04599.x

The authors examined a patient presenting with congenital sensory neuropathy with selective loss of small myelinated nerve fibres. The appearance of (bilaterial) keratitis or corneal ulceration in early childhood is strongly suggestive of congenital corneal anaesthesia. Concomitant symptoms such as anisocoria, abnormal pupillary reaction, diminished tear production and disturbed sensibility to pain and temperature point to a generalized disease: one of the hereditary sensory and autonomic neuropathies. In order to establish a definite diagnosis, elaborate neurological examination, including ultrastructural study of a muscle-nerve biopsy, is required. Tarsorrhaphy, therapeutic flushfitting PMMA scleral lenses and hydrophilic HEMA contact lenses are advocated, in order to protect the cornea. The results with high-water-content hydrophilic contact lenses are promising, those of keratoplasty limited.