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Findings in the present case were compared with those of previously reported cases. Other syndromes associated with agenesis of the corpus callosum must be differentiated. The main differences between the acrocallosal syndrome and the Greig syndrome are outlined with particular emphasis on digital anomalies. The acrocallosal syndrome is an autosomal recessive trait with variable expressivity. Hypogenitalism may be a presenting feature. Positive consanguinity provides further evidence for autosomal recessive inheritance.<\/jats:p>","DOI":"10.1002\/ajmg.1320320304","type":"journal-article","created":{"date-parts":[[2005,6,11]],"date-time":"2005-06-11T23:28:16Z","timestamp":1118532496000},"page":"301-305","source":"Crossref","is-referenced-by-count":24,"title":["Hypogenitalism in the acrocallosal syndrome"],"prefix":"10.1002","volume":"32","author":[{"given":"Samia A.","family":"Temtamy","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nagwa A.","family":"Meguid","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2005,6,5]]},"reference":[{"key":"e_1_2_1_2_1","first-page":"1103","article-title":"Le syndrome spasmes en flexion, agenesie calleuse, anomalies chorio\u2010retiniennes","volume":"26","author":"Aicardi J","year":"1969","journal-title":"Arch Fr Pediatr"},{"key":"e_1_2_1_3_1","first-page":"242","article-title":"Familial agenesis of the corpus callosum with anterior horn cell disease. 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