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  1. Article ; Online: Antenatal ultrasound features of isolated recurrent copy number variation in 7q11.23 (Williams syndrome and 7q11.23 duplication syndrome).

    Courdier, Cécile / Boudjarane, John / Malan, Valérie / Muti, Christine / Sperelakis-Beedham, Brian / Odent, Sylvie / Jaillard, Sylvie / Quelin, Chloé / Le Caignec, Cédric / Patat, Olivier / Dubucs, Charlotte / Julia, Sophie / Schluth-Bolard, Caroline / Goumy, Carole / Redon, Sylvia / Gaillard, Jean-Baptiste / Huynh, Minh Tuan / Dupont, Céline / Tabet, Anne-Claude /
    Cogan, Guillaume / Vialard, François / Dard, Rodolphe / Jedraszak, Guillaume / Jobic, Florence / Lefebvre, Mathilde / Quenum, Geneviève / Inai, Saori / Rama, Mélanie / Sauvestre, Fanny / Coatleven, Frédéric / Thomas, Julie / Rooryck, Caroline

    Prenatal diagnosis

    2023  Volume 43, Issue 6, Page(s) 734–745

    Abstract: Objective: We aimed to gather fetal cases carrying a 7q11.23 copy number variation (CNV) and collect precise clinical data to broaden knowledge of antenatal features in these syndromes.: Methods: We retrospectively recruited unrelated cases with 7q11. ...

    Abstract Objective: We aimed to gather fetal cases carrying a 7q11.23 copy number variation (CNV) and collect precise clinical data to broaden knowledge of antenatal features in these syndromes.
    Methods: We retrospectively recruited unrelated cases with 7q11.23 deletion, known as Williams-Beuren syndrome (WBS), or 7q11.23 duplication who had prenatal ultrasound findings. We collected laboratory and clinical data, fetal ultrasound, cardiac ultrasound and fetal autopsy reports from 18 prenatal diagnostic centers throughout France.
    Results: 40 fetuses with WBS were collected and the most common features were intra-uterine growth retardation (IUGR) (70.0%, 28/40), cardiovascular defects (30.0%, 12/40), polyhydramnios (17.5%, 7/40) and protruding tongue (15.0%, 6/40). Fetal autopsy reports were available for 11 cases and were compared with ultrasound prenatal features. Four cases of fetuses with 7q11.23 microduplication were collected and prenatal ultrasound signs were variable and often isolated.
    Conclusion: This work strengthens the fact that 7q11.23 CNVs are associated with a broad spectrum of antenatal presentations. IUGR and cardiovascular defects were the most frequent ultrasound signs. By reporting the biggest series of antenatal WBS, we aim to better delineate distinctive signs in fetuses with 7q11.23 CNVs.
    MeSH term(s) Humans ; Female ; Pregnancy ; Williams Syndrome/diagnostic imaging ; Williams Syndrome/genetics ; Williams Syndrome/complications ; DNA Copy Number Variations ; Retrospective Studies ; Fetal Growth Retardation ; Ultrasonography
    Language English
    Publishing date 2023-03-23
    Publishing country England
    Document type Journal Article
    ZDB-ID 82031-3
    ISSN 1097-0223 ; 0197-3851
    ISSN (online) 1097-0223
    ISSN 0197-3851
    DOI 10.1002/pd.6340
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Congenital diaphragmatic eventration and bilateral uretero-hydronephrosis in a patient with neonatal Marfan syndrome caused by a mutation in exon 25 of the FBN1 gene and review of the literature.

    Revencu, Nicole / Quenum, Geneviève / Detaille, Thierry / Verellen, Gaston / De Paepe, Anne / Verellen-Dumoulin, Christine

    European journal of pediatrics

    2004  Volume 163, Issue 1, Page(s) 33–37

    Abstract: Unlabelled: Neonatal Marfan syndrome, the most severe presentation of Marfan syndrome phenotypes (MIM 154700), is characterised mainly by joint contractures, arachnodactyly, loose skin, crumpled ears, severe atrioventricular valve dysfunction and ... ...

    Abstract Unlabelled: Neonatal Marfan syndrome, the most severe presentation of Marfan syndrome phenotypes (MIM 154700), is characterised mainly by joint contractures, arachnodactyly, loose skin, crumpled ears, severe atrioventricular valve dysfunction and pulmonary emphysema. Death usually occurs within the first 2 years of life from congestive heart failure. We describe here a newborn male with many typical characteristics of neonatal Marfan syndrome associated with a diaphragmatic eventration and a bilateral uretero-hydronephrosis with bladder dilatation. He died from cardiac failure due to severe tricuspid and mitral regurgitation at 62 h of age.
    Conclusion: Molecular analysis showed a heterozygous missense mutation at nucleotide 3165 (3165T>G) in exon 25 of the FBN1 gene, resulting in the substitution of cysteine for tryptophan (C1055W).
    MeSH term(s) Diaphragmatic Eventration/etiology ; Diaphragmatic Eventration/genetics ; Fatal Outcome ; Fibrillin-1 ; Fibrillins ; Heart Failure/etiology ; Heart Failure/genetics ; Humans ; Infant, Newborn ; Male ; Marfan Syndrome/complications ; Marfan Syndrome/genetics ; Microfilament Proteins/genetics ; Mutation, Missense ; Urologic Diseases/etiology ; Urologic Diseases/genetics
    Chemical Substances FBN1 protein, human ; Fibrillin-1 ; Fibrillins ; Microfilament Proteins
    Language English
    Publishing date 2004-01
    Publishing country Germany
    Document type Case Reports ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 194196-3
    ISSN 1432-1076 ; 0340-6199 ; 0943-9676
    ISSN (online) 1432-1076
    ISSN 0340-6199 ; 0943-9676
    DOI 10.1007/s00431-003-1330-8
    Database MEDical Literature Analysis and Retrieval System OnLINE

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