A novel mutation in MYCN gene causing congenital absence of the flexor pollicis longus tendon as an unusual presentation of Feingold syndrome 1.
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DOI: 10.1097/mcd.0000000000000342
Abstract: Feingold syndrome 1 (FGLDS1) is an autosomal dominant malformation syndrome, characterized by skeletal anomalies, microcephaly, facial dysmorphism, gastrointestinal atresias and learning disabilities. Mutations in the MYCN gene are known to be the cause of this… read more here.
Keywords: absence flexor; congenital absence; mycn gene; feingold syndrome ... See more keywords