PMC:5324983 / 4161-4933 JSONTXT

{"target":"http://pubannotation.org/docs/sourcedb/PMC/sourceid/5324983","sourcedb":"PMC","sourceid":"5324983","source_url":"https://www.ncbi.nlm.nih.gov/pmc/5324983","text":"The patient's main clinical and radiographic findings – namely narrow thorax, multiple segmentation defects of the vertebrae, malalignment of the ribs with variable points of intercostal fusion, and reduction in rib number – enabled the diagnosis of SCD with the additional features of Arnold-Chiari type II malformation, thoracolumbar meningomyelocele, and a rapidly involuting congenital hemangioma. Associated anomalies in SCD include neural tube defects, congenital heart disease, urogenital and anal anomalies, limb abnormalities, and diaphragmatic, umbilical, and inguinal hernias.3,4 However, congenital hemangioma has not been reported yet. Thus, the current observation expands the SCD phenotype and further illustrates the variable expressivity of this disorder.","tracks":[{"project":"2_test","denotations":[{"id":"28300884-8074145-2342192","span":{"begin":589,"end":590},"obj":"8074145"}],"attributes":[{"subj":"28300884-8074145-2342192","pred":"source","obj":"2_test"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"2_test","color":"#dc93ec","default":true}]}]}}