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.
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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)
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Topics |
- Acrocephalosyndactylia
(diagnosis)
- Humans
- Infant
- Male
- Polydactyly
(diagnosis)
- Toes
(pathology)
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