Recurrent anorexia and pigmentation of skin for more than two months in an infant

• Published in: Zhongguo dang dai er ke za zhi 2017-08, Vol.19 (8), p.926
• Main Authors: Zheng, Zhang-Qian, Wu, Bing-Bing, Zhang, Miao-Ying, Lu, Wei, Luo, Fei-Hong
• Format: Article
• Language: Chinese
• Subjects: Anorexia - etiology; Comparative Genomic Hybridization; Humans; Hypoadrenocorticism, Familial - complications; Hypoadrenocorticism, Familial - diagnosis; Hypoadrenocorticism, Familial - drug therapy; Infant; Male; Recurrence; Skin Pigmentation; Triglycerides - blood
• ISSN: 1008-8830
• DOI: 10.7499/j.issn.1008-8830.2017.08.015

A 2-month-old boy presented with adrenal insufficiency, impaired liver function, hypertriglyceridemia, significantly elevated creatine kinase and electrolyte disturbance. Microarray comparative genomic hybridization (aCGH) analysis test showed a pathogenic 8.7 Mb deletion in the short arm of chromosome X (Xp21.3 - p21.1) and confirmed the diagnosis of complex glycerol kinase deficiency (cGKD). He was treated with hydrocortisone, coenzyme Q10 and L-carnitine and was subsequently followed up for 4 years. His serum cortisol levels returned to normal one week later after treatment, but the serum creatine kinase, triglyceride and aminotransferase levels were progressively increased along with mental retardation and decreased muscular strength. cGKD is also named as Xp21 contiguous gene syndrome. The clinical manifestations of this disease include hypertriglyceridemia, congenital adrenal hypoplasia (AHC), Duchenne muscular dystrophy, and mental retardation. This case highlights the necessity to screen the serum tri