Arachnodactyly and Ectopia Lentis in a Father and Daughter

Arachnodactyly and Ectopia Lentis in a Father and Daughter.

Burch (1936), in a comprehensive review, was largely responsible for furthering recognition of the condition in America, and the number of cases that have been reported, mostly in the ophthalmological literature, during the past ten years is an indication that arachnodactyly is not of extreme rarity, and that many milder cases and 'formes frustes ' have previously passed unrecognized. Stewart (...

Ectopia lentis et pupillae

The Ectopia lentis et pupillae is a rare genetic syndrome, congenital, autosomal recessive with variable expression, characterized by ectopia of the lens and the pupil, usually bilateral and symmetrical, but without systemic manifestations. The pathogenesis of this anomaly is still unknown, but there are theories that the change is mesodermal, neuroectodermal, combined or mechanical. This artic...

Some Observations on Ectopia Lentis

Myositis in father and daughter.

The occurrence of myositis in a father and his daughter is reported. The daughter's illness resembled childhood dermatomyositis and progressed to systemic involvement and death less than four years from the onset of symptoms. In the case of the father the illness followed the course of adult polymyositis and there was little evidence of systemic involvement. The immunological and genetic signif...

Familial ectopia lentis and its complications.

FAMILIAL ectopia lentis is a well recognized condition and is usually seen by the ophthalmologist in its fully developed stage. It was thought worth while to record this family, as some of the very earliest stages have been observed and the complications of the condition have been very varied. The family is a large one, spread over a large part of the Union of South Africa, and it has not been ...