Crawford, P.J.M., Aldred, M. and Bloch-Zupan, A. (2007) Amelogenesis imperfect. Orphanet Journal of Rare Diseases, 2, 1-11. doi:10.1186/1750-1172-2-1
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.