| Literature DB >> 26791356 |
Steven Deimling1, Chris Sotiropoulos1, Kimberly Lau1, Sonia Chaudhry2, Kendra Sturgeon1, Simon Kelley2, Unni Narayanan2, Andrew Howard2, Chi-Chung Hui1,3, Sevan Hopyan1,2,3.
Abstract
Tibial hemimelia is a rare, debilitating and often sporadic congenital deficiency. In syndromic cases, mutations of a Sonic hedgehog (SHH) enhancer have been identified. Here we describe an ~5 kb deletion within the SHH repressor GLI3 in two patients with bilateral tibial hemimelia. This deletion results in a truncated GLI3 protein that lacks a DNA-binding domain and cannot repress hedgehog signaling. These findings strengthen the concept that tibial hemimelia arises because of failure to restrict SHH activity to the posterior aspect of the limb bud.Entities:
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Year: 2016 PMID: 26791356 DOI: 10.1038/jhg.2015.161
Source DB: PubMed Journal: J Hum Genet ISSN: 1434-5161 Impact factor: 3.172