A paediatric case of myopericarditis post-COVID-19 mRNA vaccine
Sign Up to like & getrecommendations! Published in 2022 at "Cardiology in the Young"
DOI: 10.1017/s1047951122000312
Abstract: Myopericarditis is a condition, which primarily involves the pericardium, with minimal myocardial involvement. In myopericarditis, chest pain, elevated cardiac enzymes, and electrocardiographic changes occur. Although COVID-19 mRNA vaccines significantly contribute to preventing the COVID-19 disease,… read more here.
Keywords: paediatric case; myopericarditis; covid; covid mrna ... See more keywords
Paediatric case of left subclavian artery steal syndrome with an abnormal connection between the left subclavian artery and pulmonary artery
Sign Up to like & getrecommendations! Published in 2020 at "Journal of Paediatrics and Child Health"
DOI: 10.1111/jpc.15150
Abstract: A 20-month-old boy (weight, 7.6 kg) was admitted to the hospital because of suspected right aortic arch and small patent ductus arteriosus (PDA) on colour Doppler echocardiography. The baby was born prematurely at 32 weeks… read more here.
Keywords: artery; case left; paediatric case; pulmonary artery ... See more keywords
Therapeutic challenge of a paediatric case of Graves' disease with severe ophthalmopathy
Sign Up to like & getrecommendations! Published in 2017 at "BMJ Case Reports"
DOI: 10.1136/bcr-2017-219269
Abstract: An otherwise healthy girl aged 4 years was observed because of a 6-month history of tachycardia, polyphagia, chronic cough and agitation. Physical examination revealed hiperhydrosis, exuberant exophthalmia (figure 1) and a palpable, elastic and painless… read more here.
Keywords: paediatric case; case graves; case; challenge paediatric ... See more keywords
Vascular Abnormalities and Neurofibromatosis Type 1: A Paediatric Case Series
Sign Up to like & getrecommendations! Published in 2024 at "Journal of Child Neurology"
DOI: 10.1177/08830738241284081
Abstract: Neurofibromatosis type 1 (NF1) is a multisystemic neurocutaneous disease caused by a heterozygous mutation of the NF1 gene that encodes neurofibromin. Complications include vascular and neurologic abnormalities such as moyamoya syndrome, a cerebrovascular disorder with… read more here.
Keywords: paediatric case; vascular abnormalities; type; abnormalities neurofibromatosis ... See more keywords
Isoniazid-induced gynaecomastia: report of a paediatric case and review of literature
Sign Up to like & getrecommendations! Published in 2020 at "BMC Endocrine Disorders"
DOI: 10.1186/s12902-020-00639-9
Abstract: Background Gynaecomastia is a fairly common condition in puberty but is rare in prepubertal boys. While it is necessary to exclude possible endocrinopathay in prepubertal gynaecomastia, medication is an important and potentially reversible cause to… read more here.
Keywords: paediatric case; case; report; gynaecomastia ... See more keywords
PAEDIATRIC CASE OF 3-METHYLCROTONYLGLYCINURIA WITH ENCEPHALOPATHY: A CASE REPORT FROM PAKISTAN.
Sign Up to like & getrecommendations! Published in 2024 at "Journal of Ayub Medical College, Abbottabad : JAMC"
DOI: 10.55519/jamc-01-12130
Abstract: 3-Methylcrotonylglycinuria is a common inborn error of metabolism (IEM) resulting from the deficiency of 3-Methylcrotonyl-CoA carboxylase (3-MCC) and its prevalence ranges from 1:2400 to 1:6800. The disease may be asymptomatic or may present with signs… read more here.
Keywords: paediatric case; case methylcrotonylglycinuria; case report; case ... See more keywords