Night-Blindness with Peculiar Conjunctival Changes in Children

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Night blindness and conjunctival xerosis caused by vitamin A deficiency in patients with cystic fibrosis.

Forty three patients with cystic fibrosis, aged 8-44 years (median 16 years), were examined for evidence of vitamin A deficiency. Eight patients had abnormal dark adaptation tests and three had conjunctival xerosis. Serum vitamin A and retinol binding protein concentrations were significantly lower in the affected patients who were also more likely to have abnormal liver function tests. Five pa...

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Congenital Stationary Night Blindness Panel

Test code: OP1201 The Blueprint Genetics Congenital Stationary Night Blindness Panel is a 17 gene test for genetic diagnostics of patients with clinical suspicion of congenital stationary night blindness. The panel covers genes associated with autosomal recessive, autosomal dominant and X-linked forms of congenital stationary night blindness (CSNB). The clinical utility of this diagnostic panel...

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Congenital Stationary Night Blindness Panel

Test code: OP1201 The Blueprint Genetics Congenital Stationary Night Blindness Panel is a 17 gene test for genetic diagnostics of patients with clinical suspicion of congenital stationary night blindness. The panel covers genes associated with autosomal recessive, autosomal dominant and X-linked forms of congenital stationary night blindness (CSNB). The clinical utility of this diagnostic panel...

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The Treatment of Night Blindness

The eye is cocainised as for cataract operationWith the usual aseptic precautions i c.c. of sterile 10 per cent, salt solution is injected subconjunctival^ ?n each side. Puncture of the conjunctival vessels js avoided. The eyes are bandaged. The bandage! lS removed at night, when to the satisfaction of both the doctor and the patient night blindness will be found to have disappeared. There is p...

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ژورنال

عنوان ژورنال: Proceedings of the Royal Society of Medicine

سال: 1912

ISSN: 0035-9157

DOI: 10.1177/003591571200501514