Oligoarticular Juvenile Idiopathic Arthritis | the most common JIA subtype
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Oligoarticular JIA is the most common subtype of juvenile arthritis. Children with oligo have 4 or fewer joints involved in the first 6 months of disease. The biggest complication that requires monitoring for is chronic uveitis which is asymptomatic but ultimately vision threatening if not controlled. Follow us on Instagram @yourekiddingrightdoctors Our email is [email protected] Make sure you hit SUBSCRIBE/FOLLOW so you don’t miss any episodes and RATE to help other people find us! (This isn’t individual medical advice, please use your own clinical judgement and local...
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Exomphalos | Omphalocoele
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Summary: Exomphalos, or omphalocoele, is a congenital condition where a baby's abdominal organs develop outside the body through the umbilical cord, affecting about 1 in 5000 births, with higher rates in multiple pregnancies (e.g. twins, triplets). It forms between the 6th-10th week of gestation and can be classified as minor or major based on the size of the defect. The condition is sometimes associated with genetic syndromes and other anomalies, necessitating thorough prenatal screening and multidisciplinary care. Tune in to hear more about this condition and an overview of how it is...
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Genetic Imprinting | what usually happens, and how it can go wrong
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Genetic imprinting is a normal process that usually happens in a small number of genes where one copy of the gene is always “silenced” or not expressed. An imprinting “disorder” is where there’s an issue with this process - either with how the gene is silenced or the right copy is silenced but there’s a problem with the copy that gets “expressed”. Today's episode is a doozy! This is one for all our friend's studying for their specialty exams (or keen medical students/students of other superhuman knowledge degrees!). Follow us on Instagram @yourekiddingrightdoctors...
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Congenital Diaphragmatic Hernia | an overview
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Summary: Congenital diaphragmatic hernia (CDH) is a condition where abdominal contents herniate into the thoracic cavity via a defect in the diaphragm, causing underdevelopment of the lungs and altered pulmonary vascular development. Although uncommon, it can cause significant morbidity during the neonatal period, and may continue to do so in the long term. Mortality is significant across the globe – up to 40-50%. Definitive management is operative, once the baby is stabilised. Links and resources: Follow us on Instagram @yourekiddingrightdoctors Our email is...
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Adolescent Asthma | work SMART not hard
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There has been a recent move to prescribe an inhaled corticosteroid for ALL adolescents with asthma. In today's episode we will go through the new SMART guidelines for adolescent asthma. Links and resources: Follow us on Instagram: Make sure you hit SUBSCRIBE/FOLLOW so you don’t miss out on any pearls of wisdom and RATE/REVIEW to help us grow!
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Paediatric Fasting Guidelines | when your patients are also hangry
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Meckel diverticulum
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After a decent hiatus we're back with a new episode! Meckel diverticulum is the most common congenital abnormality of the gastrointestinal tract, found in the small intestine. The majority of patients are never diagnosed, as it is both often completely asymptomatic, and difficult to spot on the usual imaging modalities. The symptoms of a Meckel's depend on the complication it presents with - and there are a range of these from bleeding to bowel obstruction. Listen in to learn about the way these elusive diverticula present if they ever reveal themselves, how to manage it and more!...
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Dermoid cysts | spot the diagnosis
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Dermoid cysts are a common occurrence and a common spot diagnosis that you'll be quizzed on in clinic! Always present at birth, but often picked up later, most cutaneous dermoid cysts are harmless, but occasionally, they may grow over time and develop complications. Tune in to learn how to tell them apart from other cutaneous lesions, their management and more! Links and resources: Follow us on Instagram @yourekiddingrightdoctors Our email is [email protected] Make sure you hit SUBSCRIBE/FOLLOW so you don’t miss any episodes and RATE to help other people find us! (This...
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Noonan Syndrome | what you need to know in 20 minutes
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Noonan syndrome is one of the most common genetic conditions we see in paeds. It is most typically characterised by certain facial features, short stature, congenital heart defects and developmental delay. Noonan syndrome is caused by a mutation in a single gene, however there are quite a few possible genes that can be responsible. Vision and hearing loss, developmental delay, development of hypertrophic cardiomyopathy and the increased risk of leukaemia are important complications to monitor for patients with Noonans.
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JDM | Juvenile Dermatomyositis
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Juvenile dermatomyositis, or JDM is a rare autoimmune myopathy. In their first episode back after sitting specialty exams, Freya and Anne use a case to help explain what JDM is, as well as presentation, treatment and diagnosis (plus a couple of tangents about their day to day work as doctors!). Follow us on Instagram @yourekiddingrightdoctors Our email is [email protected] Make sure you hit SUBSCRIBE/FOLLOW so you don’t miss any episodes and RATE to help other people find us! (This isn’t individual medical advice, please use your own clinical judgement and local...
info_outlineThe newborn hearing screen is a test conducted on all newborn babies with the aim of early detection of possible hearing problems. In this episode, we discuss how this screen works, the possible results, risk factors for hearing loss, and more.
Links and resources:
Follow us on Instagram @yourekiddingrightdoctors
Our email is [email protected]
Make sure you hit SUBSCRIBE/FOLLOW so you don’t miss any episodes and RATE to help other people find us!
(This isn’t individual medical advice, please use your own clinical judgement and local guidelines when caring for your patients)