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Frontometaphyseal dysplasia with congenital urinary tract malformations
Clinical Genetics
|December 1, 1979
Abstract:
A 12-year-old by with unusual face and hearing loss was diagnosed as having frontometaphyseal dysplasia. He also had congenital urinary tract malformations and chronic urinary tract infection. The cranial and facial bones of the patient were studied by roentgen cephalometric analysis.