Affiliations 

  • 1 Department of Paediatrics, Universiti Putra Malaysia
  • 2 Department of Diagnostic and Interventional Imaging, KK Women's and Children's Hospital, Singapore
  • 3 Department of Paediatric Endocrinology, KK Women's and Children's Hospital, Singapore
J ASEAN Fed Endocr Soc, 2020;35(1):122-124.
PMID: 33442180 DOI: 10.15605/jafes.035.01.21

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.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.