Clinical and genetic analysis of an infant with combined pituitary hormone deficiency due to POU1F1 gene variants.
10.3760/cma.j.cn511374-20190921-00486
- Author:
Qun LI
1
;
Juan LI
;
Guoying CHANG
;
Yu DING
;
Yirou WANG
;
Yongnian SHEN
;
Jian WANG
;
Xiumin WANG
Author Information
1. Department of Endocrinology and Metabolism, Shanghai Children's Medical Center, Shanghai Jiaotong University School of Medicine, Shanghai 200127, China. labwangjian@shsmu.edu.cn.
- Publication Type:Journal Article
- From:
Chinese Journal of Medical Genetics
2020;37(9):1018-1020
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the clinical characteristics and genetic basis for an infant featuring combined pituitary hormone deficiency.
METHODS:Clinical data and results of DNA sequencing of the child were analyzed.
RESULTS:The 10-month-old male infant presented with recurrent hypoglycemia, extremely poor appetite and constipation, and severe growth retardation from 2 months on, in addition with pituitary hormone deficiency involving growth hormone, thyroid stimulating hormone, and prolactin. Next generation sequencing revealed a novel heterozygous c.767-769del (p.Glu256del) variant of the POU1F1 gene in the patient.
CONCLUSION:The patient was diagnosed with combined pituitary hormone deficiency due to the POU1F1 gene variant, for which replacement therapy including thyroxine and growth hormone was provided. Hypoglycemia is unusual in patients carrying POU1F1 gene variants and requires close attention in clinical practice. For children with multiple pituitary hormone deficiency, genetic testing should be recommended to determine the cause.
