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Published in 2021 at "BMJ Case Reports"
DOI: 10.1136/bcr-2021-243164
Abstract: Myhre syndrome is a rare disorder characterised by short stature, skeletal anomalies, facial dysmorphism and hearing loss (HL), resulting from heterozygous mutations of the SMAD4 gene. We describe the benefits of cochlear implant (CI) in…
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Keywords:
cochlear implantation;
implantation patient;
patient myhre;
myhre syndrome ... See more keywords