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Catalogue of inherited disorders found among the Irish Traveller population.
Lynch, Sally Ann; Crushell, Ellen; Lambert, Deborah M; Byrne, Niall; Gorman, Kathleen; King, Mary D; Green, Andrew; O'Sullivan, Siobhan; Browne, Fiona; Hughes, Joanne; Knerr, Ina; Monavari, Ahmad A; Cotter, Melanie; McConnell, Vivienne P M; Kerr, Bronwyn; Jones, Simon A; Keenan, Catriona; Murphy, Nuala; Cody, Declan; Ennis, Sean; Turner, Jackie; Irvine, Alan D; Casey, Jillian.
  • Lynch SA; National Rare Disease Office, Mater Misericordiae University Hospital, Dublin, Republic of Ireland.
  • Crushell E; Academic Centre on Rare Diseases, University College Dublin, Dublin, Republic of Ireland.
  • Lambert DM; Academic Centre on Rare Diseases, University College Dublin, Dublin, Republic of Ireland.
  • Byrne N; National Centre for Inherited Metabolic Disorders, Temple Street Children's University Hospital, Dublin, Republic of Ireland.
  • Gorman K; National Rare Disease Office, Mater Misericordiae University Hospital, Dublin, Republic of Ireland.
  • King MD; National Rare Disease Office, Mater Misericordiae University Hospital, Dublin, Republic of Ireland.
  • Green A; Academic Centre on Rare Diseases, University College Dublin, Dublin, Republic of Ireland.
  • O'Sullivan S; Department of Neurology, Temple Street Children's University Hospital, Dublin, Republic of Ireland.
  • Browne F; Academic Centre on Rare Diseases, University College Dublin, Dublin, Republic of Ireland.
  • Hughes J; Department of Neurology, Temple Street Children's University Hospital, Dublin, Republic of Ireland.
  • Knerr I; Academic Centre on Rare Diseases, University College Dublin, Dublin, Republic of Ireland.
  • Monavari AA; Department of Paediatrics, Royal Belfast Hospital for Sick Children, Belfast, UK.
  • Cotter M; Department of Paediatric Dermatology, Our Lady's Children's Hospital, Dublin, Republic of Ireland.
  • McConnell VPM; National Centre for Inherited Metabolic Disorders, Temple Street Children's University Hospital, Dublin, Republic of Ireland.
  • Kerr B; National Centre for Inherited Metabolic Disorders, Temple Street Children's University Hospital, Dublin, Republic of Ireland.
  • Jones SA; National Centre for Inherited Metabolic Disorders, Temple Street Children's University Hospital, Dublin, Republic of Ireland.
  • Keenan C; Department of Paediatric Haematology, Temple Street Children's University Hospital, Dublin, Republic of Ireland.
  • Murphy N; Northern Ireland Regional Genetics Service, Belfast City Hospital, Belfast Health and Social Care Trust, Belfast, UK.
  • Cody D; Manchester Centre for Genomic Medicine, Central Manchester University Hospitals NHS Foundation Trust, St Mary's Hospital, Manchester, UK.
  • Ennis S; Manchester Centre for Genomic Medicine, Central Manchester University Hospitals NHS Foundation Trust, St Mary's Hospital, Manchester, UK.
  • Turner J; National Coagulation Laboratory, Central Pathology Laboratory, St. James's Hospital, Dublin, Republic of Ireland.
  • Irvine AD; Department of Paediatric Endocrinology, Temple Street Children's University Hospital, Dublin, Republic of Ireland.
  • Casey J; Department of Paediatric Endocrinology, Our Lady's Children's Hospital, Dublin, Republic of Ireland.
J Med Genet ; 55(4): 233-239, 2018 04.
Article en En | MEDLINE | ID: mdl-29358271
ABSTRACT
Background Irish Travellers are an endogamous, nomadic, ethnic minority population mostly resident on the island of Ireland with smaller populations in Europe and the USA. High levels of consanguinity result in many rare autosomal recessive disorders. Due to founder effects and endogamy, most recessive disorders are caused by specific homozygous mutations unique to this population. Key clinicians and scientists with experience in managing rare disorders seen in this population have developed a de facto advisory service on differential diagnoses to consider when faced with specific clinical scenarios. Objective(s) To catalogue all known inherited disorders found in the Irish Traveller population. Methods We performed detailed literature and database searches to identify relevant publications and the disease mutations of known genetic disorders found in Irish Travellers. Results We identified 104 genetic disorders 90 inherited in an autosomal recessive manner; 13 autosomal dominant and one a recurring chromosomal duplication. Conclusion We have collated our experience of inherited disorders found in the Irish Traveller population to make it publically available through this publication to facilitate a targeted genetic approach to diagnostics in this ethnic group.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Genética de Población / Enfermedades Genéticas Congénitas Límite: Humans País como asunto: Europa Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Genética de Población / Enfermedades Genéticas Congénitas Límite: Humans País como asunto: Europa Idioma: En Año: 2018 Tipo del documento: Article