Giraldo-Ocampo S

No ORCID on file · 1 paper in corpus
case-report 2022
Frontiers in genetics ·doi:10.3389/fgene.2022.1092301

Craniofrontonasal Syndrome is a very rare dominant X-linked genetic disorder characterized by symptoms such as hypertelorism, craniosynostosis, eye alterations, bifid nose tip, and longitudinal ridging and splitting of nails. Heterozygous f…