“…A variety of diagnoses have been suggested to explain Akhenaten's characteristics, reported as well by Hawass et al (2010), including: Marfan syndrome, Wilson-Turner X linked mental retardation syndrome, Fröhlich (adiposogenital dystrophy) syndrome, Klinefelter syndrome, androgen insensitivity syndrome, aromatase excess syndrome in conjunction with sagittal craniosynostosis syndrome, or Antley-Bixler syndrome or a variant form of that syndrome or others (Braverman et al, 2009;Farag and Iskandar, 1998;François and Cilliers, 2011;Paulshock, 1980;Walshe, 1973). Furthermore, Akhenaten's appearance could result from classical homocystinuria due to deficit of cystathionine beta-synthase characterized by the involvement of the eyes, skeleton, nervous system, and vascular system suggested by Cavka et al (2010).…”