Abstract:
:Smith-Magenis syndrome is a microdeletion syndrome involving chromosome 17p11.2. The characteristic features include mental retardation, dysmorphic facial features, minor skeletal anomalies including brachydactyly and behavioural abnormalities, such as disturbed sleep pattern, restlessness and self-destructive behaviour. We present a patient with this syndrome and with six digits on each hand. Polydactyly has not yet been described in Smith-Magenis syndrome as far as we know.
journal_name
Clin Dysmorpholjournal_title
Clinical dysmorphologyauthors
Mariannejensen L,Kirchhoff Mdoi
10.1097/00019605-200510000-00004subject
Has Abstractpub_date
2005-10-01 00:00:00pages
189-90issue
4eissn
0962-8827issn
1473-5717pii
00019605-200510000-00004journal_volume
14pub_type
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