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- W1966396323 abstract "Amelogenesis imperfecta is an unusual hereditory disorder affecting both primary and permanent dentition. We present a rare case of hypocalcified auto-somal recessive amelogenesis imperfecta occuring in primary dentition in a 7-year-old girl with a family history of consanguineous marriage. Clinical and radiological examination revealed discoloration and hypoplasia of enamel with easy chipping affecting both maxillary and mandibular dentition." @default.
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- W1966396323 date "2012-01-01" @default.
- W1966396323 modified "2023-09-30" @default.
- W1966396323 title "Hypocalcified autosomal recessive amelogenesis imperfecta—A case report" @default.
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- W1966396323 doi "https://doi.org/10.4236/ojst.2012.24044" @default.
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