Literature DB >> 19339795

A case of X-linked adrenal hypoplasia congenita, central precocious puberty and absence of the DAX-1 gene: implications for pubertal regulation.

Kah-Yin Loke1, Larry Kok-Seng Poh, Warren Wei-Rhen Lee, Poh-San Lai.   

Abstract

BACKGROUND/AIMS: X-linked adrenal hypoplasia congenita (AHC) is typically associated with DAX-1 mutations and hypogonadotropic hypogonadism. However, atypical cases of X-linked AHC in association with central precocious puberty and even normal puberty have rarely been reported, although the mechanism of action remains unknown. CASE REPORT: This is a case report of a boy with X-linked AHC associated with Duchenne muscular dystrophy, whose clinical presentation led to analysis of the DAX-1, glycerol kinase (GK1) and dystrophin genes, which were amplified by polymerase chain reaction, with Southern blot analysis of the AHC locus.
RESULTS: There was a non-contiguous deletion of the DAX-1 and GK1 genes, with deletion of the dystrophingene from exons 3 to 79.
CONCLUSION: This is the first report of X-linked AHC, central precocious puberty in the absence of the DAX-1 gene. The fact that a 'loss of function' DAX-1 mutation can be associated with hypogonadotropic hypogonadism, precocious and normal puberty, suggests that DAX-1 is but one of several transcription factors which regulate puberty, and provides further evidence that other transcription factors may interact with DAX-1 and influence gonadal regulation in a complex, but hierarchical fashion. Copyright 2009 S. Karger AG, Basel.

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Year:  2009        PMID: 19339795     DOI: 10.1159/000208804

Source DB:  PubMed          Journal:  Horm Res        ISSN: 0301-0163


  6 in total

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3.  Central precocious puberty in a patient with X-linked adrenal hypoplasia congenita and Xp21 contiguous gene deletion syndrome.

Authors:  Ji Won Koh; So Young Kang; Gu Hwan Kim; Han Wook Yoo; Jeesuk Yu
Journal:  Ann Pediatr Endocrinol Metab       Date:  2013-06-30

4.  Clinical features of congenital adrenal insufficiency including growth patterns and significance of ACTH stimulation test.

Authors:  Ji Won Koh; Gu Hwan Kim; Han Wook Yoo; Jeesuk Yu
Journal:  J Korean Med Sci       Date:  2013-10-31       Impact factor: 2.153

5.  X-Linked Adrenal Hypoplasia Congenita in a Boy due to a Novel Deletion of the Entire NR0B1 (DAX1) and MAGEB1-4 Genes.

Authors:  Aleksandra Rojek; Maciej R Krawczynski; Aleksander Jamsheer; Anna Sowinska-Seidler; Barbara Iwaniszewska; Ewa Malunowicz; Marek Niedziela
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6.  Identification and Analysis of a Novel NR0B1 Mutation in Late-Onset Adrenal Hypoplasia Congenita and Hypogonadism.

Authors:  Yutaka Hasegawa; Yoshihiko Takahashi; Yuichiro Kezuka; Wataru Obara; Yoichiro Kato; Shukuko Tamura; Ken Onodera; Toshie Segawa; Tomoyasu Oda; Marino Sato; Koji Nata; Takamasa Nonaka; Yasushi Ishigaki
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  6 in total

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