Literature DB >> 28322501

Multigenerational pedigree with STAR syndrome: A novel FAM58A variant and expansion of the phenotype.

Nicole J Boczek1,2, Teresa Kruisselbrink1,3, Margot A Cousin1,2, Patrick R Blackburn2,4, Eric W Klee1,3,5, Ralitza H Gavrilova3,6, Brendan C Lanpher3.   

Abstract

STAR syndrome is a rare X-linked dominant disorder characterized by toe Syndactyly, Telecanthus, Anogenital malformations, and Renal malformations, and is caused by loss-of-function variants in FAM58A. Our proband presented with the hallmark features of STAR syndrome, as well as some additional less typical features including tethered cord and hearing loss. The proband's mother and maternal half-sister had similar clinical histories, but had variability in phenotypic severity. Clinical whole exome sequencing revealed a novel pathogenic nonsense variant, c.651G>A (p.Trp217X; NM_152274), in FAM58A in the proband, mother, and maternal half-sister. This pedigree represents the 11-13th patients described with STAR syndrome and the third instance of familial inheritance. To our knowledge, this is the first occurrence of a nonsense variant in FAM58A described in individuals with STAR syndrome and the phenotype in this pedigree suggests that tethered cord and hearing loss are features of STAR syndrome.
© 2017 Wiley Periodicals, Inc.

Entities:  

Keywords:  FAM58A; STAR syndrome; hearing loss; tethered cord; urogenital anomalies; whole exome sequencing

Mesh:

Substances:

Year:  2017        PMID: 28322501     DOI: 10.1002/ajmg.a.38113

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  7 in total

1.  CDK10 Mutations in Humans and Mice Cause Severe Growth Retardation, Spine Malformations, and Developmental Delays.

Authors:  Christian Windpassinger; Juliette Piard; Carine Bonnard; Majid Alfadhel; Shuhui Lim; Xavier Bisteau; Stéphane Blouin; Nur'Ain B Ali; Alvin Yu Jin Ng; Hao Lu; Sumanty Tohari; S Zakiah A Talib; Noémi van Hul; Matias J Caldez; Lionel Van Maldergem; Gökhan Yigit; Hülya Kayserili; Sameh A Youssef; Vincenzo Coppola; Alain de Bruin; Lino Tessarollo; Hyungwon Choi; Verena Rupp; Katharina Roetzer; Paul Roschger; Klaus Klaushofer; Janine Altmüller; Sudipto Roy; Byrappa Venkatesh; Rudolf Ganger; Franz Grill; Farid Ben Chehida; Bernd Wollnik; Umut Altunoglu; Ali Al Kaissi; Bruno Reversade; Philipp Kaldis
Journal:  Am J Hum Genet       Date:  2017-09-07       Impact factor: 11.025

Review 2.  X-Linked Sensorineural Hearing Loss: A Literature Review.

Authors:  Virginia Corvino; Pasqualina Apisa; Rita Malesci; Carla Laria; Gennaro Auletta; Annamaria Franzé
Journal:  Curr Genomics       Date:  2018-08       Impact factor: 2.236

3.  Multimodal imaging of retinal findings in syndactyly, telecanthus, anogenital, and renal malformations (STAR) syndrome.

Authors:  Alexa L Li; Shyamanga Borooah; Eric Nudleman
Journal:  Am J Ophthalmol Case Rep       Date:  2022-01-20

Review 4.  Clinical Application of Genome and Exome Sequencing as a Diagnostic Tool for Pediatric Patients: a Scoping Review of the Literature.

Authors:  Hadley Stevens Smith; J Michael Swint; Seema R Lalani; Jose-Miguel Yamal; Marcia C de Oliveira Otto; Stephan Castellanos; Amy Taylor; Brendan H Lee; Heidi V Russell
Journal:  Genet Med       Date:  2018-05-14       Impact factor: 8.822

Review 5.  Cyclin-dependent kinases and rare developmental disorders.

Authors:  Pierre Colas
Journal:  Orphanet J Rare Dis       Date:  2020-08-06       Impact factor: 4.123

Review 6.  Cyclin-Dependent Kinases (CDK) and Their Role in Diseases Development-Review.

Authors:  Paweł Łukasik; Michał Załuski; Izabela Gutowska
Journal:  Int J Mol Sci       Date:  2021-03-13       Impact factor: 5.923

7.  Functional characterization of CDK10 and cyclin M truncated variants causing severe developmental disorders.

Authors:  Thomas Robert; Anne-Catherine Dock-Bregeon; Pierre Colas
Journal:  Mol Genet Genomic Med       Date:  2021-08-09       Impact factor: 2.183

  7 in total

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