Literature DB >> 9800907

Microcephalic osteodysplastic primordial dwarfism Taybi-Linder type: report of four cases and review of the literature.

S Sigaudy1, A Toutain, A Moncla, C Fredouille, B Bourlière, S Ayme, N Philip.   

Abstract

Microcephalic and osteodysplastic primordial dwarfism (MODP) types I, II, and III were defined by Majewski et al. in 1982. This group of syndromes was characterized by intrauterine growth retardation, microcephaly, and typical facial appearance with prominent nose and micrognathia. Type II was clearly different, both clinically and radiologically, whereas types I and III shared manifestations. Distinction between the latter two was established on the basis of subtle radiological differences. In 1967, Taybi and Linder described another syndrome with microcephalic congenital dwarfism. There is a consensus that MODP type I and III and Taybi-Linder cephaloskeletal dysplasia represent the same disorder. We report on four patients with MODP type Taybi-Linder syndromes, two of whom were born to unrelated but consanguineous parents, while the other two were sibs. Second-trimester prenatal detection by ultrasonography was possible in one case. Consanguinity in two cases and recurrence among sibs are consistent with autosomal recessive inheritance.

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Year:  1998        PMID: 9800907

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  9 in total

1.  Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC gene.

Authors:  R Nagy; H Wang; B Albrecht; D Wieczorek; G Gillessen-Kaesbach; E Haan; P Meinecke; A de la Chapelle; J A Westman
Journal:  Clin Genet       Date:  2011-08-28       Impact factor: 4.438

2.  Using genomic inbreeding coefficient estimates for homozygosity mapping of rare recessive traits: application to Taybi-Linder syndrome.

Authors:  Anne-Louise Leutenegger; Audrey Labalme; Emmanuelle Genin; Annick Toutain; Elisabeth Steichen; Francoise Clerget-Darpoux; Patrick Edery
Journal:  Am J Hum Genet       Date:  2006-04-28       Impact factor: 11.025

3.  Neuronal migration disorders in microcephalic osteodysplastic primordial dwarfism type I/III.

Authors:  Gordana Juric-Sekhar; Raj P Kapur; Ian A Glass; Mitzi L Murray; Shawn E Parnell; Robert F Hevner
Journal:  Acta Neuropathol       Date:  2010-09-21       Impact factor: 17.088

4.  Mutations in U4atac snRNA, a component of the minor spliceosome, in the developmental disorder MOPD I.

Authors:  Huiling He; Sandya Liyanarachchi; Keiko Akagi; Rebecca Nagy; Jingfeng Li; Rosemary C Dietrich; Wei Li; Nikhil Sebastian; Bernard Wen; Baozhong Xin; Jarnail Singh; Pearlly Yan; Hansjuerg Alder; Eric Haan; Dagmar Wieczorek; Beate Albrecht; Erik Puffenberger; Heng Wang; Judith A Westman; Richard A Padgett; David E Symer; Albert de la Chapelle
Journal:  Science       Date:  2011-04-08       Impact factor: 47.728

Review 5.  Primordial dwarfism: overview of clinical and genetic aspects.

Authors:  Preeti Khetarpal; Satrupa Das; Inusha Panigrahi; Anjana Munshi
Journal:  Mol Genet Genomics       Date:  2015-09-01       Impact factor: 3.291

Review 6.  Mechanisms and pathways of growth failure in primordial dwarfism.

Authors:  Anna Klingseisen; Andrew P Jackson
Journal:  Genes Dev       Date:  2011-10-01       Impact factor: 11.361

7.  A new mutation of the PCNT gene in a Colombian patient with microcephalic osteodysplastic primordial dwarfism type II: a case report.

Authors:  Harry Pachajoa; Felipe Ruiz-Botero; Carolina Isaza
Journal:  J Med Case Rep       Date:  2014-06-13

8.  Two novel mutations in RNU4ATAC in two siblings with an atypical mild phenotype of microcephalic osteodysplastic primordial dwarfism type 1.

Authors:  Anne B Krøigård; Andrew P Jackson; Louise S Bicknell; Emma Baple; Klaus Brusgaard; Lars K Hansen; Lilian B Ousager
Journal:  Clin Dysmorphol       Date:  2016-04       Impact factor: 0.816

9.  Compound heterozygous mutations in the noncoding RNU4ATAC cause Roifman Syndrome by disrupting minor intron splicing.

Authors:  Daniele Merico; Maian Roifman; Ulrich Braunschweig; Ryan K C Yuen; Roumiana Alexandrova; Andrea Bates; Brenda Reid; Thomas Nalpathamkalam; Zhuozhi Wang; Bhooma Thiruvahindrapuram; Paul Gray; Alyson Kakakios; Jane Peake; Stephanie Hogarth; David Manson; Raymond Buncic; Sergio L Pereira; Jo-Anne Herbrick; Benjamin J Blencowe; Chaim M Roifman; Stephen W Scherer
Journal:  Nat Commun       Date:  2015-11-02       Impact factor: 14.919

  9 in total

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