A novel NR0B1 mutation causes different symptoms in two patients with adrenal hypoplasia congenita
Yang Ruifei
Liu Yuanyuan
Li Yajun
Li Fanfan
Wang Jinyang
Abstract：The clinical data of 2 cases of adrenal hypoplasia congenita caused by new mutation of NR0B1 gene were reported and the literature was reviewed.
Keywords：Congenita adrenal hypoplasiaNuclear receptor subfamily 0 group B member1DiagnosisTreatment
Publication Date：2025-05-18
Online Publishing Date：2025-08-15(First online date of this platform, not the publication date of the document)
Pages：3( 616-618 )