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Lung disease in FLNA mutation: confirmatory report.
de Wit, M C Y; Tiddens, H A W M; de Coo, I F M; Mancini, G M S.
Affiliation
  • de Wit MC; Department of Pediatric Neurology, Erasmus MC-Sophia Children's Hospital, PO Box 2060, 3000 CB Rotterdam, The Netherlands. m.c.y.dewit@erasmusmc.nl
Eur J Med Genet ; 54(3): 299-300, 2011.
Article in En | MEDLINE | ID: mdl-21194575
ABSTRACT
Recently in this journal, Masurel-Paulet et al. reported the association between pulmonary disease and a mutation in X-linked FLNA in a male patient. We confirm this association in a female patient, showing that this complication is not sex-specific. Our patient has a FLNA missense mutation (c.220G > A) and presented with cerebral periventricular nodular heterotopia, cardiovascular abnormalities, and pulmonary disease consisting of lobar emphysema of the right middle pulmonary lobe with severe malacia of the right sided bronchus intermedius. Surgical resection of the right middle lobe was necessary and she had long-term oxygen dependency. Symptoms improved with age.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Contractile Proteins / Mutation, Missense / Lung Diseases / Microfilament Proteins Limits: Child, preschool / Female / Humans / Infant Language: En Journal: Eur J Med Genet Journal subject: GENETICA MEDICA Year: 2011 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Contractile Proteins / Mutation, Missense / Lung Diseases / Microfilament Proteins Limits: Child, preschool / Female / Humans / Infant Language: En Journal: Eur J Med Genet Journal subject: GENETICA MEDICA Year: 2011 Document type: Article Affiliation country: