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Autosomal recessive cutis laxa type 2A (ARCL2A) mimicking Ehlers‐Danlos syndrome by its dermatological manifestations: Report of three affected patients
Authors:Marie T. Greally  Neale N. Kalis  Wahid Agab  Kasim Ardati  Sanda Giurgea  Uwe Kornak  Lionel Van Maldergem
Affiliation:1. National Centre for Medical Genetics, Our Lady's Children's Hospital, Crumlin, Dublin, Ireland;2. Bahrain Defence Forces Hospital, Department of Paediatric Cardiology, Riffa, Kingdom of Bahrain;3. Correspondence to:;4. Marie T. Greally, M.B., FACMG., National Centre for Medical Genetics, Our Lady's Children's Hospital, Crumlin, Dublin 12, Ireland.;5. E‐mail:;6. Bahrain Specialist Hospital, Juffair, Kingdom of Bahrain;7. Department of Neurology, CHU Tivoli, La Louvière, Belgium;8. Institute of Medical and Human Genetics, Charité‐Universitaetsmedizin Berlin, Berlin, Germany;9. Centre of Human Genetics, Université de Franche‐Comté, Besan?on, France
Abstract:
Keywords:autosomal recessive cutis laxa  type 2A (ARCL2A)  ATP6V0A2‐related cutis laxa  Ehlers‐Danlos‐like skin lesions
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