Authors - Archives of Disease in Childhood
WEBAuthors who submit to Archives of Disease in Childhood and are rejected will be offered the option of transferring to BMJ Paediatrics Open. BMJ Paediatrics Open is the open access companion journal to Archives of Disease in Childhood. It is indexed by PubMed Central, Scopus, Embase, DOAJ, and Google Scholar, and publishes articles dealing with ...
About - Archives of Disease in Childhood
WEBThe content of Archives of Disease in Childhood is endorsed by the Royal College of Paediatrics and Child Health for Continued Professional Development in line with RCPCH CPD guidelines. Archives of Disease in Childhood is the flagship of BMJ’s paediatrics portfolio and has an open access companion journal, BMJ Paediatrics Open.For information about the Editor-in-Chief and editorial team ...
Understanding measures of treatment effect in clinical trials
WEBThis article discusses in a simple, practical, ‘non-statistician’ fashion some of the important outcome measures used to report clinical trials comparing different treatments or interventions. Absolute and relative risk measures are explained, and their merits and demerits discussed. The article aims to encourage healthcare professionals to ...
COVID-19 related increase in childhood tics and tic-like attacks
WEBSince the onset of the COVID-19 pandemic, paediatricians and child mental health practitioners have noticed an increase in tic symptoms in some children and adolescents already diagnosed with tic disorders.1 Interestingly, clinicians have also seen a marked increase in presentations of sudden and new onset of severe tics and ‘tic-like’ attacks. There is an urgent need to collate systematic ...
WEBMar 3, 2022 · Noonan syndrome (NS) is a mostly dominantly inherited disorder affecting 1:1000 to 1:2500 live births. The phenotype varies in severity and can involve multiple organ systems over a patient’s lifetime. Diagnosis is based on a combination of features, including typical facial features, short stature, skeletal abnormalities, presence of cardiac ...
Management of newly diagnosed diabetes: home or hospital?
WEBType 1 diabetes is one of the most common chronic childhood disorders, occurring with increasing frequency. Diabetes management involves the child and family learning how to inject insulin and monitor blood glucose, and adhere to a diet containing healthy food choices. Medical interventions necessary to stabilise newly diagnosed diabetes depend upon the clinical condition of the child at ...
Ehlers–Danlos syndrome: how to diagnose and when to perform …
WEBThe term Ehlers–Danlos syndrome (EDS) encompasses a group of inherited connective tissue disorders. The manifestations of EDS can be seen in skin, joints, blood vessels and internal organs and vary from mild to severe and life threatening. Each subtype is a separate and different condition. The genetic basis of many subtypes has now been elucidated, confirming heterogeneity.
Current evidence-based recommendations on investigating …
WEBIntroduction Global developmental delay (GDD) affects 1%–3% of the population of children under 5 years of age, making it one of the most common conditions presenting in paediatric clinics; causes are exogenous, genetic (non-metabolic) or genetic (metabolic). Recent advances in biotechnology and genetic testing mean that the investigations available to perform for children under 5 years are ...
The effect of ADHD on the life of an individual, their family, and ...
WEBAttention deficit/hyperactivity disorder (ADHD) may affect all aspects of a child’s life. Indeed, it impacts not only on the child, but also on parents and siblings, causing disturbances to family and marital functioning. The adverse effects of ADHD upon children and their families changes from the preschool years to primary school and adolescence, with varying aspects of the disorder being ...
Investigating microcephaly - Archives of Disease in Childhood
WEB1. Microcephaly is a clinical finding, not a ‘disease’, and is a crude but trusted assessment of intracranial brain volume. 2. Developmental processes reducing in utero neuron generation present at birth with ‘Primary microcephaly’. 3. ‘Secondary microcephaly’ develops after birth and predominantly reflects dendritic or white matter diseases. 4. Microcephalic conditions have a ...
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