Literature DB >> 17353728

Barth syndrome is associated with a cognitive phenotype.

Michèle M M Mazzocco1, Anne E Henry, Richard I Kelly.   

Abstract

OBJECTIVE: Barth syndrome is a rare, X-linked recessive disorder that affects only boys. The cardinal characteristics include growth retardation, cardioskeletal myopathy, chronic or cyclic neutropenia, and 3-methylglutaconic aciduria. A preliminary study of five young boys with Barth syndrome suggested a distinct cognitive phenotype.
METHODS: The present study was designed to explore whether additional evidence for a cognitive phenotype emerged from a larger sample. A psychoeducational assessment battery was administered to 15 boys with Barth syndrome. Data from these boys were compared to data from 15 typically developing boys individually matched on age and grade in school to each of the 15 boys with Barth syndrome.
RESULTS: Although boys with Barth syndrome had age-appropriate performance on all measures of reading-related skills, their performance on mathematics and visual spatial tasks was significantly lower than that of boys in the comparison group. Moreover, specific aspects of visual short-term memory also differed from available norms.
CONCLUSION: Our findings support the validity of the preliminary findings and reflect a higher incidence of cognitive difficulties in boys with Barth syndrome relative to boys in the comparison group. Coupled with the fatigue regularly experienced by boys with Barth syndrome, our findings indicate that educational support should be implemented during the early school-age years for children with Barth syndrome.

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Year:  2007        PMID: 17353728      PMCID: PMC2813702          DOI: 10.1097/01.DBP.0000257519.79803.90

Source DB:  PubMed          Journal:  J Dev Behav Pediatr        ISSN: 0196-206X            Impact factor:   2.225


  22 in total

1.  Rapid "automatized" naming (R.A.N): dyslexia differentiated from other learning disabilities.

Authors:  M B Denckla; R G Rudel
Journal:  Neuropsychologia       Date:  1976       Impact factor: 3.139

2.  Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth syndrome.

Authors:  S B Bleyl; B R Mumford; V Thompson; J C Carey; T J Pysher; T K Chin; K Ward
Journal:  Am J Hum Genet       Date:  1997-10       Impact factor: 11.025

Review 3.  X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060).

Authors:  P G Barth; R J Wanders; P Vreken; E A Janssen; J Lam; F Baas
Journal:  J Inherit Metab Dis       Date:  1999-06       Impact factor: 4.982

4.  X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria.

Authors:  R I Kelley; J P Cheatham; B J Clark; M A Nigro; B R Powell; G W Sherwood; J T Sladky; W P Swisher
Journal:  J Pediatr       Date:  1991-11       Impact factor: 4.406

5.  Preliminary evidence for a cognitive phenotype in Barth syndrome.

Authors:  M M Mazzocco; R I Kelley
Journal:  Am J Med Genet       Date:  2001-09-01

6.  Genetic analysis of the G4.5 gene in families with suspected Barth syndrome.

Authors:  A M Cantlay; K Shokrollahi; J T Allen; P W Lunt; R A Newbury-Ecob; C G Steward
Journal:  J Pediatr       Date:  1999-09       Impact factor: 4.406

7.  Barth syndrome: clinical features and confirmation of gene localisation to distal Xq28.

Authors:  L C Adès; A K Gedeon; M J Wilson; M Latham; M W Partington; J C Mulley; J Nelson; K Lui; D O Sillence
Journal:  Am J Med Genet       Date:  1993-02-01

Review 8.  X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): an update.

Authors:  Peter G Barth; Fredoen Valianpour; Valerie M Bowen; Jan Lam; Marinus Duran; Frédéric M Vaz; Ronald J A Wanders
Journal:  Am J Med Genet A       Date:  2004-05-01       Impact factor: 2.802

9.  Deficiency of tetralinoleoyl-cardiolipin in Barth syndrome.

Authors:  Michael Schlame; Jeffrey A Towbin; Paul M Heerdt; Roswitha Jehle; Salvatore DiMauro; Thomas J J Blanck
Journal:  Ann Neurol       Date:  2002-05       Impact factor: 10.422

10.  A novel X-linked gene, G4.5. is responsible for Barth syndrome.

Authors:  S Bione; P D'Adamo; E Maestrini; A K Gedeon; P A Bolhuis; D Toniolo
Journal:  Nat Genet       Date:  1996-04       Impact factor: 38.330

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  18 in total

Review 1.  Barth syndrome: cardiolipin, cellular pathophysiology, management, and novel therapeutic targets.

Authors:  Hana M Zegallai; Grant M Hatch
Journal:  Mol Cell Biochem       Date:  2021-01-07       Impact factor: 3.396

Review 2.  TAZ encodes tafazzin, a transacylase essential for cardiolipin formation and central to the etiology of Barth syndrome.

Authors:  Anders O Garlid; Calvin T Schaffer; Jaewoo Kim; Hirsh Bhatt; Vladimir Guevara-Gonzalez; Peipei Ping
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3.  Aberrant cardiolipin metabolism is associated with cognitive deficiency and hippocampal alteration in tafazzin knockdown mice.

Authors:  Laura K Cole; Jin Hee Kim; Andrew A Amoscato; Yulia Y Tyurina; Hülya Bay R; Benyamin Karimi; Tabrez J Siddiqui; Valerian E Kagan; Grant M Hatch; Tiina M Kauppinen
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4.  A mixed-methods investigation of sensory response patterns in Barth syndrome: a clinical phenotype?

Authors:  Stacey Reynolds; Consuelo M Kreider; Roxanna Bendixen
Journal:  Am J Med Genet A       Date:  2012-07       Impact factor: 2.802

5.  Psychosocial Functioning in Youth with Barth Syndrome.

Authors:  Eric A Storch; Mary Keeley; Lisa J Merlo; Jay B St Amant; Marni Jacob; Jill F Storch; Carolyn Spencer; Barry J Byrne
Journal:  Child Health Care       Date:  2009-04

Review 6.  Disruption of mitochondrial homeostasis in organic acidurias: insights from human and animal studies.

Authors:  Moacir Wajner; Stephen I Goodman
Journal:  J Bioenerg Biomembr       Date:  2011-02       Impact factor: 2.945

7.  Genetic ablation of calcium-independent phospholipase A2{gamma} leads to alterations in hippocampal cardiolipin content and molecular species distribution, mitochondrial degeneration, autophagy, and cognitive dysfunction.

Authors:  David J Mancuso; Paul Kotzbauer; David F Wozniak; Harold F Sims; Christopher M Jenkins; Shaoping Guan; Xianlin Han; Kui Yang; Gang Sun; Ibrahim Malik; Sara Conyers; Karen G Green; Robert E Schmidt; Richard W Gross
Journal:  J Biol Chem       Date:  2009-12-18       Impact factor: 5.157

8.  Loss of tafazzin results in decreased myoblast differentiation in C2C12 cells: A myoblast model of Barth syndrome and cardiolipin deficiency.

Authors:  Wenjia Lou; Christian A Reynolds; Yiran Li; Jenney Liu; Maik Hüttemann; Michael Schlame; David Stevenson; Douglas Strathdee; Miriam L Greenberg
Journal:  Biochim Biophys Acta Mol Cell Biol Lipids       Date:  2018-04-22       Impact factor: 4.698

Review 9.  Cellular functions of cardiolipin in yeast.

Authors:  Amit S Joshi; Jingming Zhou; Vishal M Gohil; Shuliang Chen; Miriam L Greenberg
Journal:  Biochim Biophys Acta       Date:  2008-08-07

Review 10.  Oxidized phospholipid signaling in traumatic brain injury.

Authors:  Tamil S Anthonymuthu; Elizabeth M Kenny; Andrew M Lamade; Valerian E Kagan; Hülya Bayır
Journal:  Free Radic Biol Med       Date:  2018-06-30       Impact factor: 7.376

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