Fig. 1From: Clinical and genetic characteristics of 42 Chinese paediatric patients with X-linked adrenal hypoplasia congenitaDiagnostic flowchart for X-linked AHC. PAI primary adrenal insufficiency; 17α-OHP 17α-hydroxyprogesterone; VLCFA very-long-chain fatty acids; ID intellectual disability; X-linked ALD X-linked adrenoleukodystrophy; PCR polymerase chain reaction; ES exome sequencing; qPCR real-time quantitative PCRBack to article page