Purpose: Identification of the gene(s) involved in plasma membrane remodelling. Identification of the circulating markers affected by the defective membrane remodelling in a collection of families with unexplained provoked hemorrhages and evaluation of their prognosis value in the assessment of the hemostatic cellular response.Hypothesis: Scott syndrome is rare a familial disorder characterized by provoked haemorrages in homozygous-type patients due to isolated membrane remodelling deficiency. Membrane remodelling is necessary for cellular hemostatic responses.
Study Type
OBSERVATIONAL
Enrollment
29
Observational study. Limited blood withdrawal. Any other intervention will be determined by the patient's clinical status.
Hôpital Antoine Béclère, Service d'Hématologie Biologique
Clamart, France
Laboratoire d'Hémostase et d'Immunologie, Centre Hospitalier
Le Mans, France
Laboratoire d'Hématologie, Hôpital Robert Debré
Reims, France
Laboratoire d'Hématologie, Hôpital de Hautepierre, Hôpitaux Universitaires de Strasbourg
Strasbourg, France
Service d'Hématologie Biologique, Hôpital Pierre Zobda Quitman
Fort-de-France, Martinique
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