Variable phenotypes in Greig cephalopolysyndactyly sydrome (GCPS) and their relevance to plastic surgery
Male
0301 basic medicine
Kruppel-Like Transcription Factors
Infant
Nerve Tissue Proteins
Acrocephalosyndactylia
Plastic Surgery Procedures
3. Good health
03 medical and health sciences
Phenotype
Child, Preschool
Mutation
Humans
DOI:
10.1007/s11845-015-1279-4
Publication Date:
2015-03-16T15:14:29Z
AUTHORS (2)
ABSTRACT
Greig cephalopolysyndactyly syndrome (GCPS) is an uncommon entity characterised by polysyndactyly and craniofacial features. The syndrome is not defined by classic signs. Instead there is a high variability in phenotypes observed. This is due to the large number of different mutations in the glioma-associated oncogene 3 (GLI3) that can give rise to the syndrome. We present a case series of five un-related individuals with GCPS treated in our hand surgery unit with different phenotype presentations of GCPS.An awareness of the diversity in phenotypes is important for diagnosis and early referral for genetic confirmation and counselling.
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CITATIONS (1)
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