Publications by authors named "Siobhan Gormally"

Article Synopsis
  • - The case involves congenital hypertrichosis linked to a duplication of the FOXN1 gene, which is located on chromosome 17 and crucial for hair growth regulation.
  • - FOXN1 is part of the forkhead box gene family, playing an important role in the differentiation of epithelial cells and specifically keratinocytes related to hair.
  • - This report is significant as it is the first documented instance of FOXN1 duplication being associated with congenital hypertrichosis in scientific literature.
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Background: In several countries, respiratory syncytial virus prophylaxis is offered to late preterm infants who are at escalated risk of respiratory syncytial virus hospitalization (RSVH). However, targeted prophylaxis should be informed by country-specific data. This study, which uniquely includes 36 weeks of gestational age (GA) infants, aims to establish the risk factors for RSVH in 32-36 weeks of GA infants in Ireland.

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Background: No midwifery-led units existed in Ireland before 2004. The aim of this study was to compare midwife-led (MLU) versus consultant-led (CLU) care for healthy, pregnant women without risk factors for labour and delivery.

Methods: An unblinded, pragmatic randomised trial was designed, funded by the Health Service Executive (Dublin North-East).

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Objectives: Recurrent abdominal pain (RAP) affects up to 15% of children. A biopsychosocial approach to the treatment of children with RAP has been proposed as an alternative to the traditional medical model. The aim of this study was to examine whether the parental conceptual model of illness is a factor in the long-term outcome of children with severe RAP.

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