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Split-Hand/Foot Malformation and Subependymal Heterotopia Caused by a DLX5 Gene Mutation: A Case Report |
Jun Hee Shin, Min Jeong Han, Sun Jun Kim |
Ann Child Neurol. 2021;29(4):199-201. Published online August 25, 2021 DOI: https://doi.org/10.26815/acn.2021.00472 |
Split-Hand/Foot Malformation and Subependymal Heterotopia Caused by a DLX5 Gene Mutation: A Case Report Split hand foot malformation: Presentation of a rare case and description of a novel technique in management of split hand Study design: Case report Split hand foot malformation is associated with a reduced level of Dactylin gene expression Split Hand Foot Malformation (SHFM) Split-hand/split-foot malformation with paternal mutation in the p63 gene Split Hand/Foot Malformation Anorectal malformation associated with a mutation in the P63 gene in a family with split hand–foot malformation Split-Hand/Split-Foot Malformation Is Caused by Mutations in the p63 Gene on 3q27 Split hand/foot malformation with long bone deficiency associated with BHLHA9 gene duplication: a case report and review of literature Split hand/split foot malformation with hearing loss: first report of families linked to the SHFM1 locus in 7q21 |