Crossed polydactyly and Greig cephalopolysyndactyly syndrome.

Abstract

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
• Journal: Indian pediatrics (Indian Pediatr) Vol. 50 Issue 10 Pg. 967-8 (Oct 2013) ISSN: 0974-7559 [Electronic] India
• PMID: 24222286 (Publication Type: Case Reports, Journal Article)

Topics

• Acrocephalosyndactylia (diagnosis)
• Humans
• Infant
• Male
• Polydactyly (diagnosis)
• Toes (pathology)