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Understanding the burden of weekly somatrogon injections compared with daily somatropin injections in children with growth hormone deficiency: a plain language summary of publication somatrogon injections were less of a burden than once-daily somatropin injections. • The safety of weekly somatrogon was similar to that of daily somatropin. • Compared with daily somatropin injections, children with growth hormone deficiency may be less likely to miss weekly somatrogon injections. ○ This is because weekly somatrogon injections were less of a burden and were less likely to interfere with daily activities compared with daily somatropin injections. The purpose of this plain language summary is to help you to understand the findings from recent research. • Somatrogon is used to treat the condition under study that is discussed in this summary. Approval varies by country; please check with your local provider for more details. • The results of this study may differ from those of other studies. Health professionals should make treatment decisions based on all available evidence and not on the results of a single study. This original scientific article on which this summary is based was published in the Journal of the Endocrine Society and can be accessed for free at: https://academic.oup.com/jes/article/6/10/bvac117/6695276. The details of the original article are as follows: Aristides K. Maniatis, Mauri Carakushansky, Sonya Galcheva, Gnanagurudasan Prakasam, Larry A. Fox, Adriana Dankovcikova, Jane Loftus, Andrew A. Palladino, Maria de los Angeles Resa, Carrie Turich Taylor, Mehul T. Dattani, Jan Lebl. Treatment burden of weekly somatrogon versus daily somatropin in children with growth hormone deficiency: a randomized study. J Endocr Soc 2022; 6(10): bvac117. DOI: 10.1210/jendso/bvac117.
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- Therapeutic Advances in Endocrinology & Metabolism, 2024, p. 1, doi. 10.1177/20420188241274363
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- Publication type:
- Article
Search for a time- and cost-saving genetic testing strategy for maturity-onset diabetes of the young.
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- Acta Diabetologica, 2022, v. 59, n. 9, p. 1169, doi. 10.1007/s00592-022-01915-x
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- Publication type:
- Article
Lessons learned from 5 years of newborn screening for congenital adrenal hyperplasia in the Czech Republic: 17-hydroxyprogesterone, genotypes, and screening performance.
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- 2012
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- Publication type:
- journal article
Lessons learned from 5 years of newborn screening for congenital adrenal hyperplasia in the Czech Republic: 17-hydroxyprogesterone, genotypes, and screening performance.
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- European Journal of Pediatrics, 2012, v. 171, n. 6, p. 935, doi. 10.1007/s00431-011-1656-6
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- Publication type:
- Article
Aortic dissection and rupture in a 16-year-old girl with Turner syndrome following previous progression of aortic dilation.
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- 2010
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- Publication type:
- journal article
Unusually severe phenotype of neonatal primary hyperparathyroidism due to a heterozygous inactivating mutation in the CASR gene.
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- 2009
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- Publication type:
- journal article
Refining clinical phenotypes in septo-optic dysplasia based on MRI findings.
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- 2008
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- Publication type:
- journal article
Pendred syndrome among patients with congenital hypothyroidism detected by neonatal screening: identification of two novel PDS/SLC26A4 mutations.
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- 2008
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- Publication type:
- journal article
Prevalence of congenital adrenal hyperplasia among sudden infant death in the Czech Republic and Austria.
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- 2007
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- Publication type:
- journal article
Absence of breast-feeding is associated with the risk of type 1 diabetes: a case-control study in a population with rapidly increasing incidence.
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- 2006
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- Publication type:
- journal article
High prevalence of coeliac disease in siblings of children with type 1 diabetes.
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- 2005
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- Publication type:
- journal article
Cerebral oedema in enuretic children during low-dose desmopressin treatment: a preventable complication.
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- 2001
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- Publication type:
- journal article
Longitudinal growth in HIV-negative boys with haemophilia.
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- 2000
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- Publication type:
- journal article
Vrozený hyperinzulinizmus: když B-buňka ztratí sebekontrolu?
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- Internal Medicine / Vnitrni Lekarstvi, 2016, v. 62, p. 4S72
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- Publication type:
- Article
Foreword.
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- Acta Paediatrica, 1995, v. 84, n. s411, p. 1, doi. 10.1111/j.1651-2227.1995.tb13849.x
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- Publication type:
- Article
Genetic Testing of Children With Familial Tall Stature: Is it Worth Doing?
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- Journal of Clinical Endocrinology & Metabolism, 2024, v. 109, n. 11, p. e2009, doi. 10.1210/clinem/dgae067
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- Publication type:
- Article
Response to Letter to the Editor from Youn Hee Jee: "Familial Short Stature - A Novel Phenotype of Growth Plate Collagenopathies".
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- Journal of Clinical Endocrinology & Metabolism, 2022, v. 107, n. 1, p. e445, doi. 10.1210/clinem/dgab665
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- Publication type:
- Article
Familial Short Stature-A Novel Phenotype of Growth Plate Collagenopathies.
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- 2021
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- Publication type:
- journal article
NPR2 Variants Are Frequent among Children with Familiar Short Stature and Respond Well to Growth Hormone Therapy.
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- 2020
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- Publication type:
- journal article
Two novel mutations in seven Czech and Slovak kindreds with familial neurohypophyseal diabetes insipidus-benefit of genetic testing.
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- 2016
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- Publication type:
- journal article
Coarctation of the aorta in Noonan-like syndrome with loose anagen hair.
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- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 5, p. 1218, doi. 10.1002/ajmg.a.36404
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- Publication type:
- Article
Nadměrný růst u dětí a dospělých: nový klinický pohled, nové geny, nové fenotypy.
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- Journal of Czech Physicians / Časopis Lékařů Českých, 2017, v. 156, n. 5, p. 233
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- Publication type:
- Article
Haplotype analysis of the X chromosome in patients with Turner syndrome in order to verify the possible effect of imprinting on selected symptoms.
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- Biomedical Papers of the Medical Faculty of Palacky University in Olomouc, 2022, v. 166, n. 1, p. 63, doi. 10.5507/bp.2020.060
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- Publication type:
- Article
A 6-Year Follow-Up of Fracture Incidence and Volumetric Bone Mineral Density Development in Girls With Turner Syndrome.
- Published in:
- 2017
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- Publication type:
- journal article
Clinical Characterization of Patients With Autosomal Dominant Short Stature due to Aggrecan Mutations.
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- 2016
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- Publication type:
- journal article
High Incidence of Heterozygous ABCC8 and HNF1A Mutations in Czech Patients With Congenital Hyperinsulinism.
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- 2015
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- Publication type:
- journal article
High prevalence of PROP1 defects in Lithuania: phenotypic findings in an ethnically homogenous cohort of patients with multiple pituitary hormone deficiency.
- Published in:
- 2014
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- Publication type:
- journal article
Paediatric diabetes subtypes in a consanguineous population: a single-centre cohort study from Kurdistan, Iraq.
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- Diabetologia, 2024, v. 67, n. 1, p. 113, doi. 10.1007/s00125-023-06030-2
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- Publication type:
- Article
De novo mutations of GCK, HNF1A and HNF4A may be more frequent in MODY than previously assumed.
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- Diabetologia, 2014, v. 57, n. 3, p. 480, doi. 10.1007/s00125-013-3119-2
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- Publication type:
- Article
Šíření nákazy SARS-CoV-2 mezi žáky základních škol: současný stav poznání.
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- Pediatrie pro Praxi, 2021, v. 22, n. 2, p. 87, doi. 10.36290/ped.2021.015
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- Publication type:
- Article
SALL4 Phenotype in Four Generations of One Family: An Interplay of the Upper Limb, Kidneys, and the Pituitary.
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- Hormone Research in Paediatrics, 2024, v. 97, n. 2, p. 203, doi. 10.1159/000531996
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- Publication type:
- Article
Integrative Role of the SALL4 Gene: From Thalidomide Embryopathy to Genetic Defects of the Upper Limb, Internal Organs, Cerebral Midline, and Pituitary.
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- Hormone Research in Paediatrics, 2024, v. 97, n. 2, p. 106, doi. 10.1159/000531452
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- Publication type:
- Article
The Genetic Landscape of Children Born Small for Gestational Age with Persistent Short Stature.
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- Hormone Research in Paediatrics, 2024, v. 97, n. 1, p. 40, doi. 10.1159/000530521
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- Publication type:
- Article
Family and Population-Based Studies of Variation within the Ghrelin Receptor Locus in Relation to Measures of Obesity.
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- PLoS ONE, 2010, v. 5, n. 4, p. 1, doi. 10.1371/journal.pone.0010084
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- Publication type:
- Article
Steroid 17alpha-hydroxylase deficiency: functional characterization of four mutations (A174E, V178D, R440C, L465P) in the CYP17A1 gene.
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- 2009
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- Publication type:
- journal article
Melanocortin 4 Receptor Mutations in Obese Czech Children: Studies of Prevalence, Phenotype Development, Weight Reduction Response, and Functional Analysis.
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- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 9, p. 3689, doi. 10.1210/jc.2007-0352
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- Publication type:
- Article
Association between Neuromedin U Gene Variants and Overweight and Obesity.
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- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 12, p. 5057, doi. 10.1210/jc.2006-1442
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- Publication type:
- Article
Continued Growth Hormone (GH) Treatment after Final Height Is Necessary to Complete Somatic Development in Childhood-Onset GH-Deficient Patients.
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- Journal of Clinical Endocrinology & Metabolism, 2004, v. 89, n. 10, p. 4857, doi. 10.1210/jc.2004-0551
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- Publication type:
- Article
Lessons From 30 Years of Clinical Diagnosis and Treatment of Congenital Adrenal Hyperplasia in Five Middle European Countries.
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- Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 7, p. 2958, doi. 10.1210/jcem.86.7.7638
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- Publication type:
- Article
Treatment Burden of Weekly Somatrogon vs Daily Somatropin in Children With Growth Hormone Deficiency: A Randomized Study.
- Published in:
- Journal of the Endocrine Society, 2022, v. 6, n. 10, p. 1, doi. 10.1210/jendso/bvac117
- By:
- Publication type:
- Article
Impact of SARS-CoV-2 variants on the incidence of paediatric inflammatory multisystem syndrome (PIMS-TS).
- Published in:
- Journal of Paediatrics & Child Health, 2022, v. 58, n. 10, p. 1901, doi. 10.1111/jpc.16204
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- Publication type:
- Article
Screening of monogenic autoimmune diabetes among children with type 1 diabetes and multiple autoimmune diseases: is it worth doing?
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 10, p. 1147, doi. 10.1515/jpem-2019-0261
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- Publication type:
- Article
Short stature in a boy with atypical progeria syndrome due to LMNA c.433G>A [p.(Glu145Lys)]: apparent growth hormone deficiency but poor response to growth hormone therapy.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 7, p. 775, doi. 10.1515/jpem-2019-0107
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- Publication type:
- Article
An isolated Xp deletion is linked to autoimmune diseases in Turner syndrome.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 5, p. 479, doi. 10.1515/jpem-2019-0067
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- Publication type:
- Article
Could a combination of heterozygous ABCC8 and KCNJ11 mutations cause congenital hyperinsulinism?
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2017, v. 30, n. 12, p. 1311, doi. 10.1515/jpem-2017-0163
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- Publication type:
- Article
MODY in Ukraine: genes, clinical phenotypes and treatment.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2017, v. 30, n. 10, p. 1095, doi. 10.1515/jpem-2017-0075
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- Publication type:
- Article
Increased prevalence of bicuspid aortic valve in Turner syndrome links with karyotype: the crucial importance of detailed cardiovascular screening.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2017, v. 30, n. 3, p. 319, doi. 10.1515/jpem-2016-0301
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- Publication type:
- Article
Low-dose insulin therapy in patients with cystic fibrosis and early-stage insulinopenia prevents deterioration of lung function: a 3-year prospective study.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 7/8, p. 449, doi. 10.1515/jpem.2011.050
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- Publication type:
- Article
HNF1A mutation presenting with fetal macrosomia and hypoglycemia in childhood prior to onset of overt diabetes.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 377, doi. 10.1515/jpem.2011.049
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- Publication type:
- Article
HNF1A mutation presenting with fetal macrosomia and hypoglycemia in childhood prior to onset of overt diabetes.
- Published in:
- 2011
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- Publication type:
- Case Study