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Identification of a novel point mutation in DAX-1 gene in a patient with adrenal hypoplasia congenita

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주제분류소아과학

초록

X-linked adrenal hypoplasia congenita caused by a mutation in NR0B1/DAX-1 is a rare inherited disorder. Patients with adrenal hypoplasia congenita are usually diagnosed with primary adrenal insufficiency in infancy or early childhood and present hypogonadotropic hypogonadism during adolescence. Our patient first presented with adrenal crisis at the age of 2 months, which was managed with glucocorticoids and mineralocorticoids. At the age of 17 years, testicular volumes of 5 mL each and a stretched penile length of 4 cm were noted. A combined pituitary function test showed a peak luteinizing hormone level of 2.68 mIU/mL, testosterone 13.5 ng/dL, confirming hypogonadotropic hypogonadism. After whole-exome sequencing, a new variant of DAX-1, c.881T>C (p.Leu294Pro), was found. He was diagnosed with X-linked adrenal hypoplasia congenita and then treated with human choriogonadotropin for the induction of spermatogenesis as well as with steroid replacement therapy.

Abstract

X-linked adrenal hypoplasia congenita caused by a mutation in NR0B1/DAX-1 is a rare inherited disorder. Patients with adrenal hypoplasia congenita are usually diagnosed with primary adrenal insufficiency in infancy or early childhood and present hypogonadotropic hypogonadism during adolescence. Our patient first presented with adrenal crisis at the age of 2 months, which was managed with glucocorticoids and mineralocorticoids. At the age of 17 years, testicular volumes of 5 mL each and a stretched penile length of 4 cm were noted. A combined pituitary function test showed a peak luteinizing hormone level of 2.68 mIU/mL, testosterone 13.5 ng/dL, confirming hypogonadotropic hypogonadism. After whole-exome sequencing, a new variant of DAX-1, c.881T>C (p.Leu294Pro), was found. He was diagnosed with X-linked adrenal hypoplasia congenita and then treated with human choriogonadotropin for the induction of spermatogenesis as well as with steroid replacement therapy.

참고문헌 (16)

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관련 논문AI추천

Primary Adrenal Insufficiency in a Newborn With Adrenal Hypoplasia Congenita Caused by a Mutation of the DAX1 Gene김성신, 박선형, 홍용희대한신생아학회 · Neonatal medicine2016 · 제23권 제1호A novel variant in NR0B1 causing X-linked adrenal hypoplasia congenitaHeo Seung, Hwang Jin Soon, Lee Hae Sang, Shim Young Suk대한소아내분비학회 · Annals of Pediatric Endocrinology & Metabolism2024 · 제29권 제3호Testicular microlithiasis in a boy with X-linked adrenal hypoplasia congenitaAnastasios Serbis, Assimina GalliTsinopoulou, Eleni P. Kotanidou, Konstantina Mouzaki, Styliani Giza, Vassiliki Regina Tsinopoulou대한소아내분비학회 · Annals of Pediatric Endocrinology & Metabolism2018 · 제23권 제3호Congenital Adrenal Agenesis Presented with Adrenal Insufficiency박홍규, 심은정, 이관섭, 황일태대한소아내분비학회 · Annals of Pediatric Endocrinology & Metabolism2012 · 제17권 제1호Two cases of 17α-hydroxylase/17,20-lyase deficiency caused by the CYP17A1 mutationChae Hyun Wook, Choi Han Saem, Kim Ho-Seong, Kwon Ahreum, Lee Hae In, Song Kyung Chul, Suh Junghwan대한소아내분비학회 · Annals of Pediatric Endocrinology & Metabolism2021 · 제26권 제1호Central precocious puberty in a patient with X-linked adrenal hypoplasia congenita and Xp21 contiguous gene deletion syndrome김구환, 유지숙, 유한욱, 황진순, Ji Won Koh, So Young Kang대한소아내분비학회 · Annals of Pediatric Endocrinology & Metabolism2013 · 제18권 제2호

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