Abstract
A 26-year-old female presented to the paediatric clinic at 11 years of age with poor growth. The detection of delayed puberty, anosmia, coloboma and hearing impairment led to a diagnosis of CHARGE syndrome. This was confirmed by a heterogenous de novo pathogenic variant c.6955C >T:p.(Arg2319Cys) detected in the CHD7 gene. Detailed assessment, including olfaction, ophthalmic and auditory examination should be part of the evaluation framework in children with delayed growth and puberty.
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Lee, Y. L., Toh, L., & Yap, F. (2020). Delayed puberty and anosmia in charge syndrome: A case report. Journal of the ASEAN Federation of Endocrine Societies, 35(1), 122–124. https://doi.org/10.15605/jafes.035.01.21
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