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Familial amyloid polyneuropathy: When does it stop to be asymptomatic and need a treatment?
Adams, D; Beaudonnet, G; Adam, C; Lacroix, C; Théaudin, M; Cauquil, C; Labeyrie, C.
Afiliación
  • Adams D; Service de neurologie, CHU Bicêtre, 78, rue du Général-Leclerc, 94275 Le Kremlin-Bicêtre cedex, France; Centre de référence national des neuropathies amyloïdes familiales et autres neuropathies périphériques rares (NNERF), 94275 Le Kremlin-Bicêtre cedex, France; Inserm U1195, 78, rue du Général-Lecl
  • Beaudonnet G; Centre de référence national des neuropathies amyloïdes familiales et autres neuropathies périphériques rares (NNERF), 94275 Le Kremlin-Bicêtre cedex, France; Unité de neurophysiologie clinique et épileptologie, CHU Bicêtre, 78, rue du Général-Leclerc, 94275 Le Kremlin-Bicêtre cedex, France.
  • Adam C; Centre de référence national des neuropathies amyloïdes familiales et autres neuropathies périphériques rares (NNERF), 94275 Le Kremlin-Bicêtre cedex, France; Service d'anatomopathologie, CHU Bicêtre, 78, rue du Général-Leclerc, 94275 Le Kremlin-Bicêtre cedex, France; Inserm U1195, 78, rue du Généra
  • Lacroix C; Centre de référence national des neuropathies amyloïdes familiales et autres neuropathies périphériques rares (NNERF), 94275 Le Kremlin-Bicêtre cedex, France; Service d'anatomopathologie, CHU Bicêtre, 78, rue du Général-Leclerc, 94275 Le Kremlin-Bicêtre cedex, France; Inserm U1195, 78, rue du Généra
  • Théaudin M; Service de neurologie, CHU Bicêtre, 78, rue du Général-Leclerc, 94275 Le Kremlin-Bicêtre cedex, France; Centre de référence national des neuropathies amyloïdes familiales et autres neuropathies périphériques rares (NNERF), 94275 Le Kremlin-Bicêtre cedex, France.
  • Cauquil C; Service de neurologie, CHU Bicêtre, 78, rue du Général-Leclerc, 94275 Le Kremlin-Bicêtre cedex, France; Centre de référence national des neuropathies amyloïdes familiales et autres neuropathies périphériques rares (NNERF), 94275 Le Kremlin-Bicêtre cedex, France.
  • Labeyrie C; Service de neurologie, CHU Bicêtre, 78, rue du Général-Leclerc, 94275 Le Kremlin-Bicêtre cedex, France; Centre de référence national des neuropathies amyloïdes familiales et autres neuropathies périphériques rares (NNERF), 94275 Le Kremlin-Bicêtre cedex, France.
Rev Neurol (Paris) ; 172(10): 645-652, 2016 Oct.
Article en En | MEDLINE | ID: mdl-27663057
Transthyretin familial amyloid polyneuropathy (FAP) is a rare disease with autosomal transmission due to point mutation of the transthyretin (TTR) gene. It is the most disabling hereditary neuropathy affecting sensory, motor and autonomic nerves, and is irreversible and fatal within 7 to 12 years of onset in the absence of therapy. Diagnosis is usually delayed for 1-5 years because the onset is usually insidious, and a positive family history is lacking in 50% of late-onset cases. Penetrance is variable, and depends of the age of the carrier and age of onset in family members. Two treatments are available: liver transplantation, to suppress the main source of systemic production of mutant TTR; and TTR tetramer stabilizer drugs, to avoid the release of highly amyloidogenic monomers and oligomers. These therapies are able to stop or slow the progression of the disease in its early stages. Genetic counseling is crucial to detect carriers at risk of developing the disease. The European network for TTR-FAP recommends careful baseline assessment by questionnaire, clinical examination and neurophysiological tests, and periodic consultations to detect the onset of disease in time to start anti-amyloid therapy after biopsy findings of amyloid deposition. A therapeutic educational program is important for improving patients' awareness. Patients are considered symptomatic and ill when they themselves perceive symptoms or changes, including changes from baseline measurements on neurophysiological tests, followed by findings of amyloid deposition on biopsy. The most sensitive biopsies are from the labial salivary gland and skin.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neuropatías Amiloides Familiares Límite: Humans Idioma: En Revista: Rev Neurol (Paris) Año: 2016 Tipo del documento: Article Pais de publicación: Francia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neuropatías Amiloides Familiares Límite: Humans Idioma: En Revista: Rev Neurol (Paris) Año: 2016 Tipo del documento: Article Pais de publicación: Francia