A Chinese child with hyperpigmentation diagnosed with familial glucocorticoid deficiency type 1 using whole-exome sequencing

• Junke Xia,
• Zhihui Jiao,
• Zhenhua Zhao,
• Jing Wu,
• Xiangdong Kong

Affiliations

Junke Xia

Center of Genetic and Prenatal Diagnosis, Zhengzhou University First Affiliated Hospital, Zhengzhou, China

Zhihui Jiao

Center of Genetic and Prenatal Diagnosis, Zhengzhou University First Affiliated Hospital, Zhengzhou, China

Zhenhua Zhao

Center of Genetic and Prenatal Diagnosis, Zhengzhou University First Affiliated Hospital, Zhengzhou, China

Jing Wu

Department of Pediatrics, Zhengzhou University First Affiliated Hospital, Zhengzhou, China

Xiangdong Kong

Corresponding author. Center of Genetic and Prenatal Diagnosis, Zhengzhou University First Affiliated Hospital, 1 Jianshe Road, Erqi District, Zhengzhou, 450052, China.; Center of Genetic and Prenatal Diagnosis, Zhengzhou University First Affiliated Hospital, Zhengzhou, China