Early-onset osteoarthritis, Charcot-Marie-Tooth like neuropathy, autoimmune features, multiple arterial aneurysms and dissections: An unrecognized and life threatening condition

PLoS ONE

Volumn 9, Issue 5, 2014, Pages

  Aubart, Mélodie ^a   Gobert, Delphine ^a   Aubart Cohen, Fleur ^b   Detaint, Delphine ^a   Hanna, Nadine ^c   D'Indya, Hyacintha ^c   Lequintrec, Janine Sophie ^a   Renard, Philippe ^a   Vigneron, Anne Marie ^a   Dieudé, Philippe ^a,d   Laissy, Jean Pierre ^a,d   Koch, Pierre ^a   Muti, Christine ^a   Roume, Joelle ^a   Cusin, Veronica ^a   Grandchamp, Bernard ^d   Gouya, Laurent ^a,e   LeGuern, Eric ^b   Papo, Thomas ^a,d   Boileau, Catherine ^c,e   Jondeau, Guillaume ^a,d   more..

^a BICHAT HOSPITAL   (France)

^b PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^c ASSISTANCE PUBLIQUE HÔPITAUX DE PARIS   (France)

^d UNIVERSITÉ PARIS DESCARTES   (France)

^e LABORATOIRE DES SCIENCES DU CLIMAT ET DE L ENVIRONNEMENT   (France)

Author keywords

[No Author keywords available]

Indexed keywords

SMAD3 PROTEIN;

ACROCYANOSIS; ADOLESCENT; ADULT; ALLERGIC ASTHMA; ALLERGIC CONJUNCTIVITIS; ALLERGIC RHINITIS; ANEURYSM; ANGIONEUROTIC EDEMA; AORTA DISEASE; AORTA DISSECTION; AORTA SURGERY; ARTHRALGIA; ARTICLE; CALCIFICATION; CHILD; CMT2 GENE; CONTROLLED STUDY; CORONARY ARTERY DISSECTION; ECZEMA; ELECTROMYOGRAPHY; ELECTRONEUROMYOGRAPHY; FAMILY; FEMALE; FIBROCARTILAGE; FOOD ALLERGY; GENE; GENE MUTATION; HASHIMOTO DISEASE; HEEL; HEREDITARY MOTOR SENSORY NEUROPATHY; HIP OSTEOARTHRITIS; HUMAN; KNEE OSTEOARTHRITIS; MALE; MIDDLE AGED; MOTOR NEUROPATHY; PERIPHERAL NEUROPATHY; PROSPECTIVE STUDY; RHEUMATOID ARTHRITIS; SENSORY NEUROPATHY; SHOULDER; SJOEGREN SYNDROME; SMAD3 GENE; SUDDEN DEATH; AGED; AUTOIMMUNE DISEASE; DISSECTING ANEURYSM; GENETICS; MUTATION; OSTEOARTHRITIS; PEDIGREE; PHENOTYPE; PRESCHOOL CHILD; SYNDROME; THORACIC AORTA ANEURYSM; YOUNG ADULT;

ADOLESCENT; ADULT; AGED; ANEURYSM, DISSECTING; AORTIC ANEURYSM, THORACIC; AUTOIMMUNE DISEASES; CHARCOT-MARIE-TOOTH DISEASE; CHILD; CHILD, PRESCHOOL; DEATH, SUDDEN; FEMALE; HUMANS; MALE; MIDDLE AGED; MUTATION; OSTEOARTHRITIS; PEDIGREE; PHENOTYPE; SMAD3 PROTEIN; SYNDROME; YOUNG ADULT;

EID: 84900556777     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0096387     Document Type: Article

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