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Witkop Jr., C.J. (1998) Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited: Problems in classification. Journal of Oral Pathology & Medicine, 17, 547-553. doi:10.1111/j.1600-0714.1988.tb01332.x

has been cited by the following article:

• TITLE: Hypocalcified autosomal recessive amelogenesis imperfecta—A case report

  AUTHORS: Ali Azhar Dawasaz, M. Zakirulla, Meer Allahbaksh

  KEYWORDS: Hypocalcified; Autosomal Recessive; Consanguineous; Discoloration

  JOURNAL NAME: Open Journal of Stomatology, Vol.2 No.4, December 7, 2012

  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.