A Rare Case of Precocious Puberty in a Child with a Novel GATA-4 Gene Mutation: Implications for Disorders of Sex Development (DSD) and Review of the Literature

Author:

Aversa Tommaso12ORCID,Luppino Giovanni12,Corica Domenico12ORCID,Pepe Giorgia12,Valenzise Mariella12,Coco Roberto12,Li Pomi Alessandra12,Wasniewska Malgorzata12ORCID

Affiliation:

1. Department of Human Pathology of Adulthood and Childhood, University of Messina, Via Consolare Valeria 1, 98125 Messina, Italy

2. Pediatric Unit, AOU Policlinico G. Martino, Via Consolare Valeria 1, 98125 Messina, Italy

Abstract

Background: Disorders/Differences of sex development (DSD) are often due to disruptions of the genetic programs that regulate gonad development. The GATA-4 gene, located on chromosome 8p23.1, encodes GATA-binding protein 4 (GATA-4), a transcription factor that is essential for cardiac and gonadal development and sexual differentiation. Case Description: A child with a history of micropenis and cryptorchidism. At 8 years of age, he came under our observation for an increase in sexual pubic hair (pubarche). The laboratory parameters and the GnRH test suggested a central precocious puberty (CPP). Treatment with GnRH analogs was started, and we decided to perform genetic tests for DSD. The NGS genetic investigation showed a novel and heterozygous variant in the GATA-4 gene. Discussion: In the literature, 26 cases with 46,XY DSD due to the GATA4 gene were reported. Conclusion: The novel variant in the GATA-4 gene of our patient was not previously associated with DSD. This is the first case of a DSD due to a GATA-4 mutation that develops precocious puberty. Precocious puberty could be associated with DSD and considered a prelude to hypogonadism in some cases.

Publisher

MDPI AG

Subject

Genetics (clinical),Genetics

Reference27 articles.

1. Lawson Wilkins Pediatric Endocrine Society/European Society for Paediatric Endocrinology Consensus Group; Consensus statement on management of intersex disorders;Hughes;J. Pediatr. Urol.,2006

2. Disorders of sex development;Witchel;Best Pract. Res. Clin. Obstet. Gynaecol.,2018

3. Sexual Developmental Disorders in Pediatrics;Profeta;Clin. Ter.,2022

4. Specific clinical and hormonal features of the non-classical form of 21-hydroxilase deficiency in the children during the first year of life detected from the results of neonatal screening;Tyulpakov;Probl. Endocrinol.,2014

5. Management of disorders of sex development;Olaf;Nat. Rev. Endocrinol.,2014

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