Spherophakia
National Institutes of Health
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Spherophakia (SP) is a rare disabling developmental disease, which commonly is seen in both eyes associated with high lenticular…
Glaucoma is the most important cause of permanent visual loss in spherophakia. Determining an appropriate procedure for the…
Weill Marchesani syndrome is a rare systemic connective tissue disease characterized by short stature, brachydactyly, ectopia…
Case report: We report the case of a child short in stature with brachydactyly and brachymorphy who was referred to our office…
Case report: We report the case of a child short in stature with brachydactyly and brachymorphy who was referred to our office…
Weill-Marchesani syndrome is a rare, generalized disorder of connective tissue manifested by short stature, brachymorphia, and…
We studied a one-year-old child with multiple malformations and a tandem duplication of the distal two-thirds of 13q. The overall…
The authors report the case of a patient with spherophakia and brachymorphism (Marchesani syndrome). This congenital and familial…
In 1939 Marchesani 1 described a syndrome consisting of brachydactyly, spherophakia, and glaucoma in four patients. Since then 27…
SOME investigators, Fuchs 1 for example, have called attention to certain congenital anomalies of the glaucomatous eyeball. A…