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Maghreb Medical. 2006; 26 (378): 87-89
in French | IMEMR | ID: emr-78959

ABSTRACT

The Roberts syndrome is a rare syndrome characterized by a severe growth deficiency, a midfacial defect with hypomelia. The authors report the first and only three Tunisian cases described until now, with a review of the literature


Subject(s)
Humans , Male , Female , Ectromelia , Face/abnormalities , Syndrome , Review , Infant, Newborn , Infant, Newborn, Diseases
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