Publication | Closed Access
Skeletal abnormalities in Rett syndrome: Increasing evidence for dysmorphogenetic defects
27
Citations
10
References
1995
Year
Rett SyndromePathologyMetacarpal AbnormalitiesOsteoporosisOrthopaedic SurgeryBone DiseaseWestern AustraliaMendelian DisorderOsteoarthritisDown SyndromeSkeletal AbnormalitiesSclerodermaDevelopmental AnomalyThumb HypoplasiaDevelopmental BiologyGenetic DisorderPediatricsMedicineConnective Tissue Disease
The presence of metatarsal and metacarpal abnormalities in some individuals has raised the possibility that Rett syndrome is, in fact, a multiple congenital abnormalities/mental retardation (MCA/MR) syndrome. We have conducted radiological examination of 17 cases of Rett syndrome in Western Australia. Short fourth and/or fifth metatarsals were identified in 65% of cases and short fourth and/or fifth metacarpals in 57%. Metatarsal (P = 0.045) and metacarpal (P = 0.006) shortness were significantly more common in girls 14 years or older. Negative ulnar variance (found in 79% of cases) appeared to be independent of age. Reduced bone density in the hands was found in 86% of cases. A nationwide study using the Australian Rett Syndrome Database is planned to follow up these findings and compare them with findings from a control group. The confirmation of these abnormalities in a high proportion of cases may provide morphologic markers to assist in the diagnosis of Rett syndrome and perhaps provide a further avenue of research into the pathogenesis of this disorder.
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