Introduction: Dentin dysplasia is a rare autosomal dominant inheriting disturbance of dentin formation characterized by normal enamel formation, but atypical dentin with abnormal pulpal morphology. There are two major patterns: type I and type II. Amelogenesis imperfecta is an autosomal dominant. X-link inherent disease that is classified by clinical manifestation into hypoplastic, hyp...

purpose: to describe the clinical and photographic features of a patient who developed left homo-nymous hemianopia due to right occipital lobe hemorrhage after ingestion of sildenafil citrate (viagra). case report: a 63-year-old man was referred for acute blurred of vision in both eyes five hours after taking 50 mg viagra® (sildenafil citrate). visual field testing revealed left homonymous hemi...

dentin dysplasia is an exceptionally rare, autosomal-dominant, hereditary condition, primarily characterized by defective dentin formation affecting both the deciduous and permanent dentitions. the etiology remains imprecise to date, in spite of the numerous hypotheses put forward and the constant updates on this condition. this case report of type i dentin dysplasia exhibits radiographic fi nd...