"Freiberger, Tom\u00E1\u0161" . . "Novel FBN1 gene mutation and maternal germinal mosaicism as the cause of neonatal form of Marfan syndrome" . . "RIV/00216224:14740/14:00079336!RIV15-MSM-14740___" . . . "US - Spojen\u00E9 st\u00E1ty americk\u00E9" . "Baxov\u00E1, A." . "http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.36480/epdf" . "14740" . "Novel FBN1 gene mutation and maternal germinal mosaicism as the cause of neonatal form of Marfan syndrome" . "Novel FBN1 gene mutation and maternal germinal mosaicism as the cause of neonatal form of Marfan syndrome"@en . "Grodeck\u00E1, Lucie" . "Mazurov\u00E1, Svatava" . "Cibulkov\u00E1, P." . "2"^^ . . "AMERICAN JOURNAL OF MEDICAL GENETICS PART A" . . "Novel FBN1 gene mutation and maternal germinal mosaicism as the cause of neonatal form of Marfan syndrome"@en . . . . "6" . "10"^^ . . "[549BBFE71F2D]" . "6"^^ . "\u0160\u00EDpek, A." . "33091" . . "Magner, Michal" . "Marfan syndrome (MFS) is an autosomal dominant disorder caused by mutations in the fibrillin 1 gene (FBN1). Neonatal form of MFS is rare and is associated with severe phenotype and a poor prognosis. We report on a newborn girl with neonatal MFS who displayed cyanosis and dyspnea on the first day of life. The main clinical features included mitral and tricuspid valve insufficiency, aortic root dilatation, arachnodactyly, and loose skin. Despite the presence of severe and inoperable heart anomalies, the girl was quite stable on symptomatic treatment and lived up to the 7th month of age when she died due to cardiorespiratory failure. Molecular-genetic studies revealed a novel intronic c.4211-32_-13del mutation in the FBN1 gene. Subsequent in vitro splicing analysis showed this mutation led to exon 35 skipping, presumably resulting in a deletion of 42 amino acids (p.Leu1405_Asp1446del)."@en . "Marfan syndrome (MFS) is an autosomal dominant disorder caused by mutations in the fibrillin 1 gene (FBN1). Neonatal form of MFS is rare and is associated with severe phenotype and a poor prognosis. We report on a newborn girl with neonatal MFS who displayed cyanosis and dyspnea on the first day of life. The main clinical features included mitral and tricuspid valve insufficiency, aortic root dilatation, arachnodactyly, and loose skin. Despite the presence of severe and inoperable heart anomalies, the girl was quite stable on symptomatic treatment and lived up to the 7th month of age when she died due to cardiorespiratory failure. Molecular-genetic studies revealed a novel intronic c.4211-32_-13del mutation in the FBN1 gene. Subsequent in vitro splicing analysis showed this mutation led to exon 35 skipping, presumably resulting in a deletion of 42 amino acids (p.Leu1405_Asp1446del)." . "Dvo\u0159\u00E1kov\u00E1, M." . "Honz\u00EDk, Tom\u00E1\u0161" . . "Zeman, J." . . "1552-4825" . "000335926600028" . . . "164" . "I, P(ED1.1.00/02.0068), S" . . . . "RIV/00216224:14740/14:00079336" . "10.1002/ajmg.a.36480" . . "neonatal Marfan syndrome; FBN1; fibrillin-1; splicing; splicing mutation"@en . .