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Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) Myopathy Misdiagnosed as Polymyositis

Barp, Andrea MD*; Bellance, Rémi MD; Malfatti, Edoardo MD, PhD‡§; Rigal, Odile PharmD; Acquaviva-Bourdain, Cécile PhD; Laforet, Pascal MD, PhD

doi: 10.1097/RHU.0000000000001000
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From the *Neurology Clinic, Gorizia Hospital, Gorizia, Italy; and

Neuromuscular Reference Center, CHU Fort-de-France, Fort de France;

Neurology Department, Raymond-Poincaré Teaching Hospital, Centre de référence des Maladies Neuromusculaires Nord/Est/Ile-de-France, AP-HP, Garches;

§Unité de Morphologie Neuromusculaire, Institut de Myologie, GHU La Pitié-Salpêtrière; and

Centre de Référence Maladies Métaboliques–Service Biochimie Hormonologie APHP- Hôpital Robert Debré, Paris; and

Service Maladies Héréditaires du Métabolisme, Centre de biologie et Pathologie Est, Groupement Hospitalier Est, CHU Lyon, Bron, France.

Correspondence: Andrea Barp, MD, Neurology Clinic, Gorizia Hospital, Via Fatebenefratelli 34, 34170, Gorizia, Italy. E-mail: andrea.barp1985@libero.it.

The authors declare no conflict of interest.

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