Russell-Silver Dwarfism Latest Advances

Clinical and genetic analysis of children with Silver-Russell syndrome

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: April 01, 2026

Comparison of bone age between both limbs in patients with congenital hemihyperplasia or hemihypoplasia: A retrospective study.

Journal: Journal of children's orthopaedics

Published: January 16, 2026

A novel CEP57 gene mutation in mosaic variegated aneuploidy syndrome 2: case report.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: November 10, 2025

Copy Number Variants in the 11p15.5 Associated Imprinting Disorders: An Attempt to Establish a Genotype-Phenotype Correlation.

Journal: Clinical genetics

Published: October 30, 2025

Assessment of combined growth hormone and gonadotropin-releasing hormone analogue treatment in children with Silver-Russell syndrome.

Journal: Hormone research in paediatrics

Published: October 17, 2025

Hypomethylation of the MEG8:Int2-DMR in patients with pathogenic PLAG1 variants suggests new role of the chr14q32 imprinting cluster in Silver-Russell syndrome.

Journal: Clinical epigenetics

Published: September 23, 2025

Imprinting Disorders and Epigenetic Alterations in Children Conceived by Assisted Reproductive Technologies: Mechanisms, Clinical Outcomes, and Prenatal Diagnosis.

Journal: Genes

Published: September 17, 2025

PEG10 loss of function causes Silver-Russell syndrome: a familial case with paternal deletion.

Journal: Scientific reports

Published: September 09, 2025

Gastrointestinal symptoms and quality of life in adults with Silver-Russell syndrome: a cross-sectional study.

Journal: Archives of disease in childhood

Published: September 05, 2025

Fetal Isolated Unilateral Multicystic Dysplastic Kidney Identified on Second Trimester Ultrasound: Genetic Investigation Results at a Single Referral Center.

Journal: Prenatal diagnosis

Published: August 09, 2025

Consensus on diagnosis and treatment of Silver-Russell syndrome (2025)

Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics

Published: June 15, 2025

Investigation of methylation profiles in Silver-Russell syndrome to explore episignatures.

Journal: Clinical epigenetics

Published: May 28, 2025

Russell-Silver Dwarfism Latest Advances

Find the Latest Research About Russell-Silver Dwarfism

Clinical and genetic analysis of children with Silver-Russell syndrome

Clinical and genetic analysis of children with Silver-Russell syndrome

Comparison of bone age between both limbs in patients with congenital hemihyperplasia or hemihypoplasia: A retrospective study.

Comparison of bone age between both limbs in patients with congenital hemihyperplasia or hemihypoplasia: A retrospective study.

A novel CEP57 gene mutation in mosaic variegated aneuploidy syndrome 2: case report.

A novel CEP57 gene mutation in mosaic variegated aneuploidy syndrome 2: case report.

Copy Number Variants in the 11p15.5 Associated Imprinting Disorders: An Attempt to Establish a Genotype-Phenotype Correlation.

Copy Number Variants in the 11p15.5 Associated Imprinting Disorders: An Attempt to Establish a Genotype-Phenotype Correlation.

Assessment of combined growth hormone and gonadotropin-releasing hormone analogue treatment in children with Silver-Russell syndrome.

Assessment of combined growth hormone and gonadotropin-releasing hormone analogue treatment in children with Silver-Russell syndrome.

Hypomethylation of the MEG8:Int2-DMR in patients with pathogenic PLAG1 variants suggests new role of the chr14q32 imprinting cluster in Silver-Russell syndrome.

Hypomethylation of the MEG8:Int2-DMR in patients with pathogenic PLAG1 variants suggests new role of the chr14q32 imprinting cluster in Silver-Russell syndrome.

Imprinting Disorders and Epigenetic Alterations in Children Conceived by Assisted Reproductive Technologies: Mechanisms, Clinical Outcomes, and Prenatal Diagnosis.

Imprinting Disorders and Epigenetic Alterations in Children Conceived by Assisted Reproductive Technologies: Mechanisms, Clinical Outcomes, and Prenatal Diagnosis.

PEG10 loss of function causes Silver-Russell syndrome: a familial case with paternal deletion.

PEG10 loss of function causes Silver-Russell syndrome: a familial case with paternal deletion.

Gastrointestinal symptoms and quality of life in adults with Silver-Russell syndrome: a cross-sectional study.

Gastrointestinal symptoms and quality of life in adults with Silver-Russell syndrome: a cross-sectional study.

Fetal Isolated Unilateral Multicystic Dysplastic Kidney Identified on Second Trimester Ultrasound: Genetic Investigation Results at a Single Referral Center.

Fetal Isolated Unilateral Multicystic Dysplastic Kidney Identified on Second Trimester Ultrasound: Genetic Investigation Results at a Single Referral Center.

Consensus on diagnosis and treatment of Silver-Russell syndrome (2025)

Consensus on diagnosis and treatment of Silver-Russell syndrome (2025)

Investigation of methylation profiles in Silver-Russell syndrome to explore episignatures.

Investigation of methylation profiles in Silver-Russell syndrome to explore episignatures.