Literature DB >> 15289771

Activating GNAS1 gene mutations in patients with premature thelarche.

Rossana Román1, Mara Cecilia Johnson, Ethel Codner, Mara Angélica Boric, Alejandra áVila, Fernando Cassorla.   

Abstract

OBJECTIVE: To identify GNAS1 gene mutations in girls with exaggerated and/or chronic fluctuating thelarche for at least 1-year duration with no other signs of precocious puberty, skeletal dysplasia, or typical skin lesions of McCune-Albright syndrome. STUDY
DESIGN: We studied the GNAS1 gene mutation by allele-specific polymerase chain reaction and enzymatic digestion in leukocyte DNA in 23 girls previously described.
RESULTS: Fluctuating thelarche was present in 14 girls and exaggerated thelarche was observed in 9. Molecular study revealed that 6 girls had a substitution of arginine by histidine in codon 201 (R201H [+]). Three R201H (+) girls reached their menarche at a mean chronologic age of 10.8 years and 9 of the R201H (-) girls at a mean age of 11 years.
CONCLUSIONS: Activating mutations of GNAS1 gene may be observed in some girls with chronic fluctuating and/or exaggerated thelarche, without other classic signs of McCune-Albright syndrome.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15289771     DOI: 10.1016/j.jpeds.2004.05.025

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  2 in total

1.  Clinical, biological and genetic analysis of prepubertal isolated ovarian cyst in 11 girls.

Authors:  Raja Brauner; Anu Bashamboo; Sébastien Rouget; Marie Goulet; Pascal Philibert; Hélène Sarda-Thibault; Christine Trivin; Micheline Misrahi; Charles Sultan; Ken McElreavey
Journal:  PLoS One       Date:  2010-06-25       Impact factor: 3.240

2.  Is premature thelarche in the first two years of life transient?

Authors:  Ahmet Uçar; Nurçin Saka; Firdevs Baş; Rüveyde Bundak; Hülya Günöz; Feyza Darendeliler
Journal:  J Clin Res Pediatr Endocrinol       Date:  2012-09
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.