| Literature DB >> 6979303 |
C S Bartsocas, P M Zeis, M Elia, C J Papadatos.
Abstract
a 12 1/2-year-old boy with the rare autosomal recessive syndrome of osteoporosis with pseudoglioma is reported. Pertinent laboratory findings included osteoporotic lesions of the skeleton and calcification of the left lens. He was hypotonic and presented atrophic globes with opacities of the lenses. His psychomotor development was normal. Parental consanguinity is not excluded.Entities:
Mesh:
Year: 1982 PMID: 6979303
Source DB: PubMed Journal: Ann Genet ISSN: 0003-3995