Literature DB >> 9475596

Mental retardation, "coarse" face, and hyperbreathing: confirmation of the Pitt-Hopkins syndrome.

I D Van Balkom1, S Quartel, R C Hennekam.   

Abstract

We present a patient with distinctive clinical manifestations resembling those first described by Pitt and Hopkins in 1978 [Aust Pediatr J 14:182-184] as a separate entity. Cardinal findings in this syndrome are mental retardation, "coarse" face, and an abnormal breathing pattern. The symptoms in this patient are different from those in the Joubert syndrome, Rett syndrome, Rett-like variants, and of a case reported by Leifer et al. [1991: Dysmorph Clin Genet 5:42-47]. The manifestations in our patient and in the case described by Singh [1993: J Paediatric Child Health 29:156-157] seem to confirm the delineation of this syndrome the cause of which remains unknown.

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Year:  1998        PMID: 9475596     DOI: 10.1002/(sici)1096-8628(19980123)75:3<273::aid-ajmg9>3.0.co;2-r

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


  9 in total

1.  The course of awake breathing disturbances across the lifespan in Rett syndrome.

Authors:  Daniel C Tarquinio; Wei Hou; Jeffrey L Neul; Gamze Kilic Berkmen; Jana Drummond; Elizabeth Aronoff; Jennifer Harris; Jane B Lane; Walter E Kaufmann; Kathleen J Motil; Daniel G Glaze; Steven A Skinner; Alan K Percy
Journal:  Brain Dev       Date:  2018-04-12       Impact factor: 1.961

2.  Pitt-Hopkins syndrome: report of a case with a TCF4 gene mutation.

Authors:  Grazia Taddeucci; Alice Bonuccelli; Ilaria Mantellassi; Alessandro Orsini; Enrico Tarantino
Journal:  Ital J Pediatr       Date:  2010-02-02       Impact factor: 2.638

3.  The role of the TCF4 gene in the phenotype of individuals with 18q segmental deletions.

Authors:  Minire Hasi; Bridgette Soileau; Courtney Sebold; Annice Hill; Daniel E Hale; Louise O'Donnell; Jannine D Cody
Journal:  Hum Genet       Date:  2011-06-14       Impact factor: 4.132

4.  Mutations in TCF4, encoding a class I basic helix-loop-helix transcription factor, are responsible for Pitt-Hopkins syndrome, a severe epileptic encephalopathy associated with autonomic dysfunction.

Authors:  Jeanne Amiel; Marlene Rio; Loic de Pontual; Richard Redon; Valerie Malan; Nathalie Boddaert; Perrine Plouin; Nigel P Carter; Stanislas Lyonnet; Arnold Munnich; Laurence Colleaux
Journal:  Am J Hum Genet       Date:  2007-03-23       Impact factor: 11.025

5.  Haploinsufficiency of TCF4 causes syndromal mental retardation with intermittent hyperventilation (Pitt-Hopkins syndrome).

Authors:  Christiane Zweier; Maarit M Peippo; Juliane Hoyer; Sergio Sousa; Armand Bottani; Jill Clayton-Smith; William Reardon; Jorge Saraiva; Alexandra Cabral; Ina Gohring; Koen Devriendt; Thomy de Ravel; Emilia K Bijlsma; Raoul C M Hennekam; Alfredo Orrico; Monika Cohen; Alexander Dreweke; Andre Reis; Peter Nurnberg; Anita Rauch
Journal:  Am J Hum Genet       Date:  2007-03-23       Impact factor: 11.025

6.  Pitt-Hopkins Syndrome.

Authors:  M Peippo; J Ignatius
Journal:  Mol Syndromol       Date:  2011-12-29

Review 7.  Pitt-Hopkins Syndrome and Differential Diagnosis: A Molecular and Clinical Challenge.

Authors:  Giuseppe Marangi; Marcella Zollino
Journal:  J Pediatr Genet       Date:  2015-09-25

8.  Prevalence of treated autism spectrum disorders in Aruba.

Authors:  Ingrid D C van Balkom; Michaeline Bresnahan; Marrit F Vogtländer; Daphne van Hoeken; Ruud B Minderaa; Ezra Susser; Hans W Hoek
Journal:  J Neurodev Disord       Date:  2009-04-14       Impact factor: 4.025

Review 9.  Pitt-Hopkins Syndrome: intellectual disability due to loss of TCF4-regulated gene transcription.

Authors:  J David Sweatt
Journal:  Exp Mol Med       Date:  2013-05-03       Impact factor: 8.718

  9 in total

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