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Robin sequence with facial and digital anomalies in two half-brothers by the same mother
D Chitayat1, C M Meunier, K A Hodgkinson
1Department of Pediatrics, Montreal Children's Hospital, Quebec, Canada.
American Journal of Medical Genetics
|August 1, 1991
Abstract:
Two half-brothers by the same mother presented with the Robin sequence and facial and digital anomalies. The mother has a normal face and mild hyperopia without abnormality on radiographs of the hands, feet, and pelvis. The older son is 4 years and the younger is 6 months old. Both have normal psychomotor development. To the best of our knowledge this familial association has not been reported before and probably represents a previously unrecognized heritable malformation syndrome. The occurrence of the syndrome in 2 half-brothers by the same unaffected mother suggests X-linked recessive inheritance.