Diagnosis and Management (Summary)

Child, Anne H.

doi:10.1007/978-1-4471-5442-6_2

Diagnosis and Management of Marfan Syndrome 2016

DOI: 10.1007/978-1-4471-5442-6_2

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Diagnosis and Management (Summary)

Anne H. Child

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Cited by 2 publications

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“…Up to 100% of patients with MFS have an abnormal cardiovascular system predisposing to increased mortality and morbidity [5]. Echocardiography is the mainstay of cardiological assessment for patients with MFS [6].…”

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confidence: 99%

Are patients with ectopia lentis known to cardiology services?

Maghsoudlou

Khanam

Banerjee

et al. 2018

Eye

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I was interested to read the paper by Chin et al. [1] that looked at the association of Chlamydia trachomatis ompA genovars and trachoma phenotypes. In their study in Ethiopia, they found that the 93 B genotypes were somewhat more likely to be associated with more severe disease than the 258A genotypes that they identified. Although their report is brief, they may be interested in studies done in a non-human primate mode that did show that there is not only some variation between different serovars in the clinical response they induce, but also some variation within different strains of serovar [2]. At the time this previous work was done, it was not possible to genotype isolates and so the genetic variation is unknown, although the clinical variation is also quite marked.

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confidence: 99%

Are patients with ectopia lentis known to cardiology services?

Maghsoudlou

Khanam

Banerjee

et al. 2018

Eye

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Inherited aortopathy: considerations for pregnancy and paediatric patients

Mamombe,

Renwick,

Potterton

et al. 2023

British Journal of Cardiac Nursing

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This article is the fifth instalment of a wider series on genetic concepts in cardiovascular medicine. While the previous instalment gave an overview of inherited aortopathies, this article discusses specific considerations for children and pregnant patients with these genetic conditions. This includes pharmacology for children and issues related to surgical intervention in paediatric care. The process of transitioning from paediatric to adult services will also be considered, as this is a key stage for the growing number of patients with inherited aortopathy who reach adulthood, with many opportunities for optimising wellbeing and quality of life. The discussion of pregnancy for patients with inherited aortopathies will include key physiological changes that occur in each trimester, with emphasis on pre-conception counselling and careful management. A case study is provided to further illustrate these points and the key role of the nurse throughout the lifespan of patients with inherited aortopathies.

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Diagnosis and Management (Summary)

Cited by 2 publications

References 13 publications

Are patients with ectopia lentis known to cardiology services?

Are patients with ectopia lentis known to cardiology services?

Inherited aortopathy: considerations for pregnancy and paediatric patients

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