Literature DB >> 3585935

Endocardial fibroelastosis: possible X linked inheritance.

S Hodgson, A Child, M Dyson.   

Abstract

We report a pedigree in which six males died of cardiac failure within the first eight months of life. These males were related through healthy females, as with X linked recessive inheritance. There was no consanguinity. None of the affected boys had an anatomical cardiac abnormality. In two affected brothers, histological evidence for endomyocardial fibroelastosis was documented, and in one of these electron microscopy demonstrated abnormalities of the mitochondria as found in mitochondrial cytopathy. A review of published reports revealed five similar X linked pedigrees, and in two of these mitochondrial abnormalities were found. We suggest that these families may show an X linked recessive cardiomyopathy with mitochondrial abnormalities.

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Year:  1987        PMID: 3585935      PMCID: PMC1049997          DOI: 10.1136/jmg.24.4.210

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  7 in total

1.  ENDOCARDIAL FIBROELASTOSIS.

Authors:  J O FORFAR; R A MILLER; A D BAIN; W MACLEOD
Journal:  Br Med J       Date:  1964-07-04

2.  Two cases of endocardial fibroelastosis--possible x-linked determination.

Authors:  R H Lindenbaum; P S Andrews; A S Khan
Journal:  Br Heart J       Date:  1973-01

3.  Familial occurrence of the contracted form of endocardial fibroelastosis.

Authors:  D E Fixler; R B Cole; M H Paul; M Lev; D A Girod
Journal:  Am J Cardiol       Date:  1970-08       Impact factor: 2.778

4.  Endocardial fibroelastosis: family studies with special reference to counseling.

Authors:  S Chen; M W Thompson; V Rose
Journal:  J Pediatr       Date:  1971-09       Impact factor: 4.406

5.  Heredity in primary endocardial fibroelastosis.

Authors:  M Westwood; R Harris; J L Burn; A J Barson
Journal:  Br Heart J       Date:  1975-10

6.  An X-linked recessive cardiomyopathy with abnormal mitochondria.

Authors:  H B Neustein; P R Lurie; B Dahms; M Takahashi
Journal:  Pediatrics       Date:  1979-07       Impact factor: 7.124

7.  An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes.

Authors:  P G Barth; H R Scholte; J A Berden; J M Van der Klei-Van Moorsel; I E Luyt-Houwen; E T Van 't Veer-Korthof; J J Van der Harten; M A Sobotka-Plojhar
Journal:  J Neurol Sci       Date:  1983-12       Impact factor: 3.181

  7 in total
  7 in total

1.  Mutation characterization and genotype-phenotype correlation in Barth syndrome.

Authors:  J Johnston; R I Kelley; A Feigenbaum; G F Cox; G S Iyer; V L Funanage; R Proujansky
Journal:  Am J Hum Genet       Date:  1997-11       Impact factor: 11.025

Review 2.  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

3.  X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome.

Authors:  A K Gedeon; M J Wilson; A C Colley; D O Sillence; J C Mulley
Journal:  J Med Genet       Date:  1995-05       Impact factor: 6.318

4.  Possible X linked congenital mitochondrial cardiomyopathy in three families.

Authors:  K H Orstavik; F Skjörten; M Hellebostad; P Hågå; A Langslet
Journal:  J Med Genet       Date:  1993-04       Impact factor: 6.318

5.  MR findings of endocardial fibroelastosis in children.

Authors:  Enno Stranzinger; Gregory J Ensing; Ramiro J Hernandez
Journal:  Pediatr Radiol       Date:  2008-01-03

6.  Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28.

Authors:  P A Bolhuis; G W Hensels; T J Hulsebos; F Baas; P G Barth
Journal:  Am J Hum Genet       Date:  1991-03       Impact factor: 11.025

Review 7.  Disorders of phospholipid metabolism: an emerging class of mitochondrial disease due to defects in nuclear genes.

Authors:  Ya-Wen Lu; Steven M Claypool
Journal:  Front Genet       Date:  2015-02-03       Impact factor: 4.599

  7 in total

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