Fig. 3From: Combined pituitary hormone deficiency harboring CHD7 gene missense mutation without CHARGE syndrome: a case reportThe concept of CHD7-associated syndrome. CHD7 mutations can have a continuous phenotypic spectrum depending on the severity of hypopituitarism and CHARGE features. HH, congenital hypogonadotropic hypogonadism; CHD7, chromodomain-helicase-DNA-binding protein 7; CPHD, combined pituitary hormone deficiencyBack to article page