Evidence of amelogenesis imperfecta in an early African Homo erectus.

J Hum Evol

Laboratory of Bio-anthropology and Ancient DNA, Hebrew University, Hadassah Faculty of Dental Medicine, Jerusalem, P.O. Box 12272, Jerusalem, Israel.

Published: June 2004

AI Article Synopsis

  • The teeth of the Homo erectus child from Ethiopia show signs of enamel dysplasia, reduced enamel density, and significant wear, resembling a hereditary condition called amelogenesis imperfecta (AI).
  • Scanning Electron Microscopy confirmed that these enamel defects were developmental issues, not results of environmental changes.
  • This finding suggests that the Garba IV child represents the earliest known case of AI, bridging the gap between evolutionary studies and genetic research.

Article Abstract

The teeth of the Homo erectus child (Garba IV) recovered from Melka Kunture Ethiopia and dated to 1.5 Ma are characterized by generalized enamel dysplasia, reduced enamel radio-opacity, and severe attrition. This combination of features is found in a large group of hereditary, generalized enamel dysplasias known as amelogenesis imperfecta (AI). SEM studies carried out on epoxy replicas of teeth from the Garba IV child, confirmed that the defects noted were developmental and not due to diagenesis. The enamel prism arrangement is abnormal and there are deep vertical furrows lacking enamel on both buccal and lingual surfaces of all molars. The lesions differ from those characteristic of linear enamel hypoplasia that form discrete horizontal lesions or pits within otherwise normal enamel. We propose that the Garba IV child is the earliest example of AI and provides a link between palaeoanthropology and molecular biology in investigations of the evolutionary history of genetic disorders.

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Source
http://dx.doi.org/10.1016/j.jhevol.2004.02.005DOI Listing

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