Muscle and Bone Impairment in Children With Marfan Syndrome: Correlation With Age andFBN1Genotype

Author:

Haine Elsa1,Salles Jean-Pierre12,Khau Van Kien Philippe3,Conte-Auriol Françoise24,Gennero Isabelle25,Plancke Aurélie3,Julia Sophie6,Dulac Yves7,Tauber Maithé12,Edouard Thomas12

Affiliation:

1. Endocrine, Bone Diseases, and Genetics Unit, Children's Hospital; Toulouse University Hospital; Toulouse France

2. INSERM UMR 1043, Centre of Pathophysiology of Toulouse Purpan (CPTP); University of Toulouse Paul Sabatier; Toulouse France

3. Medical Genetics Unit; Nîmes University Hospital, CHU Carémeau; Nîmes France

4. Pediatric Clinical Investigation Center; Children's Hospital; Toulouse University Hospital; Toulouse France

5. Biochemical Laboratory; Institut Fédératif de Biologie; Toulouse University Hospital; Toulouse France

6. Genetics Unit; Toulouse University Hospital; Toulouse France

7. Cardiology Unit; Children's Hospital; Toulouse University Hospital; Toulouse France

Publisher

Wiley

Subject

Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

Reference50 articles.

1. Marfan's syndrome;Judge;Lancet,2005

2. Marfan syndrome: from molecular pathogenesis to clinical treatment;Ramirez;Curr Opin Genet Dev.,2007

3. Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndrome;Habashi;Science,2006

4. Characteristics of children and young adults with Marfan syndrome and aortic root dilation in a randomized trial comparing atenolol and losartan therapy;Lacro;Am Heart J.,2013

5. Bone lessons from Marfan syndrome and related disorders: fibrillin, TGF-β and BMP at the balance of too long and too short;Loeys;Pediatr Endocrinol Rev,2013

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