Literature DB >> 24899006

Autism: a rare presentation of Bardet-Biedl syndrome.

Seshadri Sekhar Chatterjee1, Prathama Guha1, Arunansu Talukdar2, Gargi Dasgupta1.   

Abstract

Although mental retardation is generally associated with Bardet-Biedl (BBS) syndrome, a rare autosomal recessive disorder with multisystem involvement, autism is an unusual comorbidity. An 8-year-old boy presented to our psychiatry department with poor social skills and night blindness. On further assessment autism, mild mental retardation, retinitis pigmentosa, polydactyly and syndactyly, obesity, micropenis, maldescended testis, hypodontia and high-arched palate were noted and subsequently a diagnosis of BBS was made. To the best of our knowledge, this is the first reported case of BBS with autism from eastern India; it also emphasises the importance of thorough physical examination even in a patient presenting with pure psychiatric symptoms. 2014 BMJ Publishing Group Ltd.

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Year:  2014        PMID: 24899006      PMCID: PMC4054480          DOI: 10.1136/bcr-2014-203882

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  8 in total

1.  Behavioural phenotype of Bardet-Biedl syndrome.

Authors:  S Barnett; S Reilly; L Carr; I Ojo; P L Beales; T Charman
Journal:  J Med Genet       Date:  2002-12       Impact factor: 6.318

2.  New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population survey.

Authors:  P L Beales; N Elcioglu; A S Woolf; D Parker; F A Flinter
Journal:  J Med Genet       Date:  1999-06       Impact factor: 6.318

3.  Electroretinography and diagnosis of the Laurence-Moon-Bardet-Biedl syndrome in childhood.

Authors:  L Prosperi; M Cordella; S Bernasconi
Journal:  J Pediatr Ophthalmol       Date:  1977 Sep-Oct

4.  Toward objective classification of childhood autism: Childhood Autism Rating Scale (CARS).

Authors:  E Schopler; R J Reichler; R F DeVellis; K Daly
Journal:  J Autism Dev Disord       Date:  1980-03

5.  Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport.

Authors:  Oliver E Blacque; Michael J Reardon; Chunmei Li; Jonathan McCarthy; Moe R Mahjoub; Stephen J Ansley; Jose L Badano; Allan K Mah; Philip L Beales; William S Davidson; Robert C Johnsen; Mark Audeh; Ronald H A Plasterk; David L Baillie; Nicholas Katsanis; Lynne M Quarmby; Stephen R Wicks; Michel R Leroux
Journal:  Genes Dev       Date:  2004-07-01       Impact factor: 11.361

6.  The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndrome.

Authors:  J S Green; P S Parfrey; J D Harnett; N R Farid; B C Cramer; G Johnson; O Heath; P J McManamon; E O'Leary; W Pryse-Phillips
Journal:  N Engl J Med       Date:  1989-10-12       Impact factor: 91.245

Review 7.  Clinical features of Bardet-Biedl syndrome.

Authors:  G Ozer; B Yüksel; D Süleymanova; E Alhan; N Demircan; N Onenli
Journal:  Acta Paediatr Jpn       Date:  1995-04

8.  Use of Indian scale for assessment of autism in child guidance clinic: an experience.

Authors:  Suravi Patra; Priti Arun
Journal:  Indian J Psychol Med       Date:  2011-07
  8 in total
  1 in total

1.  Generation and characterization of Ccdc28b mutant mice links the Bardet-Biedl associated gene with mild social behavioral phenotypes.

Authors:  Matías Fabregat; Sofía Niño-Rivero; Sabrina Pose; Magdalena Cárdenas-Rodríguez; Mariana Bresque; Karina Hernández; Victoria Prieto-Echagüe; Geraldine Schlapp; Martina Crispo; Patricia Lagos; Natalia Lago; Carlos Escande; Florencia Irigoín; Jose L Badano
Journal:  PLoS Genet       Date:  2022-06-02       Impact factor: 6.020

  1 in total

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