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A novel single base deletion at codon 434 (1301delT) of the DAX1 gene associated with prepubertal testis enlargement.

作者信息

Argente Jesús, Ozisik Gokhan, Pozo Jesús, Teresa Muñoz M, Soriano-Guillén Leandro, Larry Jameson J

机构信息

Department of Pediatrics, Autonomous University Medical School, Hospital Universitario Infantil Niño Jesús, Avda. Menéndez Pelayo, 65, E-28009, Madrid, Spain.

出版信息

Mol Genet Metab. 2003 Jan;78(1):79-81. doi: 10.1016/s1096-7192(02)00198-1.

Abstract

We have identified a novel DAX1 frameshift mutation (1301delT) at codon 434 in a patient with primary adrenal insufficiency. This 11-day-old boy was admitted to the hospital with hyponatremia, hyperkalemia, and suspected congenital adrenal abnormality. He exhibited severe hypoglycemia, pallor of the skin, buccal and genital hyperpigmentation, hypotension (90/45 mm Hg), anemia, and diarrhea. Although basal gonadotropins were low, and responded minimally to exogenous GnRH, the size of his testes began to increase at age 4 and reached 4.5 mL at the age of 9 years and 8 months. Testosterone levels were prepubertal. These findings further emphasize the variable clinical presentation in children with DAX1 gene mutations and indicate the value of genetic testing in boys with primary adrenal insufficiency.

摘要

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