Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5589089 | European Journal of Medical Genetics | 2017 | 5 Pages |
Abstract
It was understood that after finding this mutation, when bone mineral density was measured with DXA in the family whose ages range between 19 and 28 and who have no bone problem before, osteoporosis was diagnosed. It was also understood that microphthalmia found in this family is a clinical finding of OPPG syndrome.
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Authors
Sezen Guntekin Ergun, Guvem Gumus Akay, Mehmet Ali Ergun, E. Ferda Perçin,