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Combined pituitary hormone deficiency harboring CHD7 gene missense mutation without CHARGE syndrome: a case report.

Yoshinari ObataKana TakayamaHideyuki NishikuboAoki TobimatsuIzumi MatsudaYuhei UeharaYumiko MaruoHiroyuki ShoMotohiro KosugiTetsuyuki Yasuda
Published in: BMC endocrine disorders (2023)
We report a rare case of CPHD harboring CHD7 mutation without CHARGE syndrome. This case provides valuable insights into phenotypes caused by CHD7 mutations. CHD7 mutations can have a continuous phenotypic spectrum depending on the severity of hypopituitarism and CHARGE features. Therefore, we would like to propose a novel concept of CHD7-associated syndrome.
Keyphrases
  • rare case
  • case report
  • solar cells
  • genome wide
  • copy number