Journal
CLINICAL DYSMORPHOLOGY
Volume 14, Issue 4, Pages 189-190Publisher
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/00019605-200510000-00004
Keywords
Smith-Magenis syndrome; polyclactyly
Categories
Ask authors/readers for more resources
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.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available