Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Observational Study
. 2022 Aug 24:13:975511.
doi: 10.3389/fendo.2022.975511. eCollection 2022.

Pubertal timing in children with Silver Russell syndrome compared to those born small for gestational age

Affiliations
Observational Study

Pubertal timing in children with Silver Russell syndrome compared to those born small for gestational age

Giuseppa Patti et al. Front Endocrinol (Lausanne). .

Erratum in

Abstract

Context: Data on pubertal timing in Silver Russell syndrome (SRS) are limited.

Design and methods: Retrospective observational study including twenty-three SRS patients [11p15 loss of methylation, (11p15 LOM, n=10) and maternal uniparental disomy of chromosome 7 (mUPD7, n=13)] and 21 small for gestational age (SGA). Clinical (thelarche in females; testis volume ≥ 4 ml in males; pubarche), BMI SD trend from the age of 5 to 9 years to the time of puberty, biochemical parameters of puberty onset [Luteinizing hormone (LH), 17-β-estradiol, testosterone], and bone age progression were evaluated.

Results: Pubertal onset and pubarche occurred significantly earlier in children with SRS than in SGA (p 0.03 and p 0.001, respectively) and clinical signs of puberty onset occurred earlier in mUPD7 than in 11p15LOM group (p 0.003). Five SRS children experienced central precocious puberty and LH, 17-β-estradiol, testosterone were detected earlier in SRS than in SGA (p 0.01; p 0.0001). Bone age delay in SRS children was followed by rapid advancement; the delta between bone age and chronological age in SRS group became significantly higher than in SGA group at the age of 9-11 years (p 0.007). 11p15LOM patients were underweight at the age of 5 years and showed a progressive normalization of BMI that was significantly higher than in mUPD7 (p 0.04) and SGA groups (p 0.03) at puberty onset.

Conclusion: Timing of puberty is affected in SRS and occurred earlier in mUPD7 compared to 11p15LOM. The impact of early puberty on adult height and metabolic status deserves long-term evaluation.

Keywords: 11p15 LOM; bone age; mUPD7; puberty; silver russell syndrome.

PubMed Disclaimer

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
BMI trend in SRS and in SGA subjects.

Similar articles

Cited by

References

    1. Wakeling EL. Silver-Russell syndrome. Arch Dis Child (2011) 96(12):1156–61. doi: 10.1136/adc.2010.190165 - DOI - PubMed
    1. Wakeling EL, Brioude F, Lokulo-Sodipe O, O' Connell SM, Salem J, Bliek J, et al. . Diagnosis and management of silver-Russell syndrome: first international consensus statement. Nat Rev Endocrinol (2017) 13(2):105–24. doi: 10.1038/nrendo.2016.138 - DOI - PubMed
    1. Neuheuser L, Meyer R, Begemann M, Elbracht M, Eggermann T. Next generation sequencing and imprinting disorders, current applications and future perspectives: Lessons from silver-Russell syndrome. Mol Cell Probes (2019) 44:1–7. doi: 10.1016/j.mcp.2018.12.007 - DOI - PubMed
    1. Abi Habib W, Brioude F, Edouard T, Bennett JT, Lienhardt-Roussie A, Tixier F, et al. . Genetic disruption of the oncogenic HMGA2-PLAG1-IGF2 pathway causes fetal growth restriction. Genet Med (2018) 20(2):250–8. doi: 10.1038/gim.2017.105 - DOI - PMC - PubMed
    1. Geoffron S, Abi Habib W, Chantot-Bastaraud S, Dubern B, Steunou V, Azzi S, et al. . Chromosome 14q32.2 imprinted region disruption as an alternative molecular diagnosis of silver-Russell syndrome. J Clin Endocrinol Metab (2018) 103(7):2436–46. doi: 10.1210/jc.2017-02152 - DOI - PubMed

Publication types