Literature DB >> 29928181

DeSanto-Shinawi Syndrome: First Case in South America.

Sara Vanegas1, Diana Ramirez-Montaño1, Estephania Candelo1, Marwan Shinawi2, Harry Pachajoa1,3.   

Abstract

Pathogenic variants in WAC are uncommon causes of developmental delay and neurobehavioral phenotypes. The clinical features associated with WAC haploinsufficiency include recognizable dysmorphic facial features that were recently delineated as DeSanto-Shinawi syndrome (DESSH; OMIM 616708). Additional clinical features include hypotonia, hearing and vision abnormalities, gastrointestinal problems, and behavioral difficulties. Here, we report a case of a 4-year-old Colombian male patient with typical dysmorphic facial features, developmental delay, hyperactivity, and recurrent respiratory infections. His immune workup revealed hypogammaglobulinemia, and clinical exome sequencing revealed a novel intronic variant in WAC (c.1437+1G>A). To the best of our knowledge, this is the first case of DESSH in South America, underlining the accumulating evidence of the significant role of WAC haploinsufficiency in neurobehavioral phenotypes. Although this report suggested the potential involvement of WAC in immune regulation, additional reports are required to confirm our observations.

Entities:  

Keywords:  Dysmorphic facial features; Intellectual disability; WAC

Year:  2018        PMID: 29928181      PMCID: PMC6006642          DOI: 10.1159/000488815

Source DB:  PubMed          Journal:  Mol Syndromol        ISSN: 1661-8769


  15 in total

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Review 4.  Autophagy in immunity: implications in etiology of autoimmune/autoinflammatory diseases.

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7.  Diagnostic exome sequencing in persons with severe intellectual disability.

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Journal:  N Engl J Med       Date:  2012-10-03       Impact factor: 91.245

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Authors:  Dorien Lugtenberg; Margot R F Reijnders; Michaela Fenckova; Emilia K Bijlsma; Raphael Bernier; Bregje W M van Bon; Eric Smeets; Anneke T Vulto-van Silfhout; Danielle Bosch; Evan E Eichler; Heather C Mefford; Gemma L Carvill; Ernie M H F Bongers; Janneke Hm Schuurs-Hoeijmakers; Claudia A Ruivenkamp; Gijs W E Santen; Arn M J M van den Maagdenberg; Cacha M P C D Peeters-Scholte; Sabine Kuenen; Patrik Verstreken; Rolph Pfundt; Helger G Yntema; Petra F de Vries; Joris A Veltman; Alexander Hoischen; Christian Gilissen; Bert B A de Vries; Annette Schenck; Tjitske Kleefstra; Lisenka E L M Vissers
Journal:  Eur J Hum Genet       Date:  2016-01-13       Impact factor: 4.246

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2.  Functional dissection of inherited non-coding variation influencing multiple myeloma risk.

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Journal:  Nat Commun       Date:  2022-01-10       Impact factor: 17.694

3.  Phenotypic comparison of patients affected with DeSanto-Shinawi syndrome: Point mutations in WAC gene versus a 10p12.1 microdeletion including WAC.

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4.  A Novel WAC Loss of Function Mutation in an Individual Presenting with Encephalopathy Related to Status Epilepticus during Sleep (ESES).

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Journal:  Genes (Basel)       Date:  2020-03-24       Impact factor: 4.096

  4 in total

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