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Evidence of mosaicism in SPAST variant carriers in four French families.
Angelini, Chloé; Goizet, Cyril; Said, Samia Ait; Camu, William; Depienne, Christel; Heron, Bénédicte; Kol, Bophara; Guillaud-Bataille, Marine; Pennamen, Perrine; Rooryck, Caroline; Scherer-Gagou, Clarisse; Tissier, Laurène; Stevanin, Giovanni; Leguern, Eric; Banneau, Guillaume.
Afiliação
  • Angelini C; Service de Génétique Médicale, CHU Bordeaux, Bordeaux, Bordeaux, France.
  • Goizet C; Centre de Référence Maladies Rares Neurogénétique, Service de Génétique Médicale, Bordeaux, France.
  • Said SA; Service de Génétique Médicale, CHU Bordeaux, Bordeaux, Bordeaux, France.
  • Camu W; Centre de Référence Maladies Rares Neurogénétique, Service de Génétique Médicale, Bordeaux, France.
  • Depienne C; INSERM U1211, laboratoire MRGM, Univ. Bordeaux, Bordeaux, France.
  • Heron B; Sorbonne Université, AP-HP, GH Pitié-Salpêtrière, Département de génétique, Paris, France.
  • Kol B; Centre de référence SLA, explorations neurologiques, CHU et Univ Montpellier, Montpellier, France.
  • Guillaud-Bataille M; Sorbonne Université, AP-HP, GH Pitié-Salpêtrière, Département de génétique, Paris, France.
  • Pennamen P; Sorbonne université, Institut du Cerveau, INSERM U 1127, Paris, France.
  • Rooryck C; Institute of Human Genetics, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
  • Scherer-Gagou C; Service de Neurologie Pédiatrique, Hôpital Armand Trousseau-La Roche Guyon, GHUEP, APHP, Paris, France.
  • Tissier L; Sorbonne Université, AP-HP, GH Pitié-Salpêtrière, Département de génétique, Paris, France.
  • Stevanin G; Sorbonne Université, AP-HP, GH Pitié-Salpêtrière, Département de génétique, Paris, France.
  • Leguern E; Service de Génétique Médicale, CHU Bordeaux, Bordeaux, Bordeaux, France.
  • Banneau G; INSERM U1211, laboratoire MRGM, Univ. Bordeaux, Bordeaux, France.
Eur J Hum Genet ; 29(7): 1158-1163, 2021 07.
Article em En | MEDLINE | ID: mdl-33958741
Hereditary spastic paraplegias (HSP) are heterogeneous disorders, with more than 70 causative genes. Variants in SPAST are the most frequent genetic etiology and are responsible for spastic paraplegia type 4 (SPG4). Age at onset can vary, even between patients from the same family, and incomplete penetrance is described. Somatic mosaicism is extremely rare with only three patients reported in the literature. We report here SPAST mosaic variants in four unrelated patients. We confirm that mosaicism in SPAST is a very rare event with only four identified cases on more than 300 patients with a SPAST variant previously described by our clinical diagnostic laboratory.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária / Espastina / Heterozigoto / Mosaicismo / Mutação Tipo de estudo: Prognostic_studies Limite: Child / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Eur J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária / Espastina / Heterozigoto / Mosaicismo / Mutação Tipo de estudo: Prognostic_studies Limite: Child / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Eur J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: França