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Crossed polydactyly and greig cephalopolysyndactyly syndrome.
MedLine Citation:
PMID:  24222286     Owner:  NLM     Status:  In-Data-Review    
Abstract/OtherAbstract:
Greig cephalopolysyndactyly syndrome is a rare genetic disorder, with an autosomal dominant inheritance and consisting of a triad of polysyndactyly, macrocephaly and hypertelorism. Crossed polydactyly is a finding characteristically associated with this syndrome. We report a one and half year old male child who presented with classic clinical features and family history diagnostic of the above syndrome.
Authors:
R Uppuluri; K Gowrishankar; L Janakiraman
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Indian pediatrics     Volume:  50     ISSN:  0974-7559     ISO Abbreviation:  Indian Pediatr     Publication Date:  2013 Oct 
Date Detail:
Created Date:  2013-11-13     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  2985062R     Medline TA:  Indian Pediatr     Country:  India    
Other Details:
Languages:  eng     Pagination:  967-8     Citation Subset:  IM    
Affiliation:
Departments of Pediatrics and *Medical Genetics, Kanchi Kamakoti Childs Trust Hospital, 12-A, Nageswara Road, Nungambakkam, Chennai, India. Correspondence to: Dr Ramya Uppuluri, House No. 26, 4th Cross Street, Dhandeeswaram Nagar, Velachery, Chennai 600 042, India. ramya.december@gmail.com.
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