Literature DB >> 7616539

Hereditary myopathy with lactic acidosis, succinate dehydrogenase and aconitase deficiency in northern Sweden: a genealogical study.

U Drugge1, M Holmberg, G Holmgren, B G Almay, H Linderholm.   

Abstract

A hereditary myopathy with lactic acidosis during physical exercise, low physical work capacity, and paroxysmal myoglobinuria (HML), called "Myopathy with deficiency of succinate dehydrogenase and aconitase" (McKusick 255125) has been described in 19 members of nine families who lived in two geographically separate areas in northern Sweden. By using the unique Swedish historical archives, including Catechetical Meeting Records from a number of northern Swedish parishes, it has been possible to trace ancestors of the nine families including all known 19 cases back in time to some key couples, who lived up to 300 years ago (that is seven to ten generations). No common single couple or common links between families in the past was found in these registers as a support for a single or several mutations that had developed far back in time. The mode of inheritance in this family is most likely autosomal recessive. This material will be used for the chromosomal localisation of the gene.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 7616539      PMCID: PMC1050427          DOI: 10.1136/jmg.32.5.344

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


  12 in total

1.  HEREDITARY METABOLIC MYOPATHY WITH PAROXYSMAL MYOGLOBINURIA DUE TO ABNORMAL GLYCOLYSIS.

Authors:  L E LARSSON; H LINDERHOLM; R MUELLER; T RINGQVIST; R SOERNAES
Journal:  J Neurol Neurosurg Psychiatry       Date:  1964-10       Impact factor: 10.154

2.  [Hereditary myopathy with succinate dehydrogenase deficiency--a rare life-threatening disease].

Authors:  H Linderholm; B G Almay; U Bäcklund; B Stegmayr; L E Thornell
Journal:  Lakartidningen       Date:  1992-04-08

3.  Hereditary abnormal muscle metabolism with hyperkinetic circulation during exercise.

Authors:  H Linderholm; R Müller; T Ringqvist; R Sörnäs
Journal:  Acta Med Scand       Date:  1969-03

4.  Familial amyloidotic polyneuropathy in Sweden: geographical distribution, age of onset, and prevalence.

Authors:  A Sousa; R Andersson; U Drugge; G Holmgren; O Sandgren
Journal:  Hum Hered       Date:  1993 Sep-Oct       Impact factor: 0.444

5.  Amino acid metabolism in patients with a hereditary myopathy and paroxysmal myoglobinuria.

Authors:  J Wahren; H Linderholm; P Felig
Journal:  Acta Med Scand       Date:  1979

6.  Low succinate dehydrogenase (SDH) activity in a patient with a hereditary myopathy with paroxysmal myoglobinuria.

Authors:  H Linderholm; B Essén-Gustavsson; L E Thornell
Journal:  J Intern Med       Date:  1990-07       Impact factor: 8.989

7.  Familial amyloidotic polyneuropathy in Sweden: a pedigree analysis.

Authors:  U Drugge; R Andersson; F Chizari; M Danielsson; G Holmgren; O Sandgren; A Sousa
Journal:  J Med Genet       Date:  1993-05       Impact factor: 6.318

8.  Computer-simulation methods in human linkage analysis.

Authors:  J Ott
Journal:  Proc Natl Acad Sci U S A       Date:  1989-06       Impact factor: 11.205

9.  Dependence of maximum performance time on work intensity in patients with a hereditary myopathy with succinate dehydrogenase deficiency.

Authors:  H Linderholm
Journal:  Clin Physiol       Date:  1992-09

10.  Deficiency of skeletal muscle succinate dehydrogenase and aconitase. Pathophysiology of exercise in a novel human muscle oxidative defect.

Authors:  R G Haller; K G Henriksson; L Jorfeldt; E Hultman; R Wibom; K Sahlin; N H Areskog; M Gunder; K Ayyad; C G Blomqvist
Journal:  J Clin Invest       Date:  1991-10       Impact factor: 14.808

View more
  8 in total

1.  Tissue specificity of a human mitochondrial disease: differentiation-enhanced mis-splicing of the Fe-S scaffold gene ISCU renders patient cells more sensitive to oxidative stress in ISCU myopathy.

Authors:  Daniel R Crooks; Suh Young Jeong; Wing-Hang Tong; Manik C Ghosh; Hayden Olivierre; Ronald G Haller; Tracey A Rouault
Journal:  J Biol Chem       Date:  2012-10-03       Impact factor: 5.157

Review 2.  Iron-sulfur cluster biogenesis in mammalian cells: New insights into the molecular mechanisms of cluster delivery.

Authors:  Nunziata Maio; Tracey A Rouault
Journal:  Biochim Biophys Acta       Date:  2014-09-19

3.  Splice mutation in the iron-sulfur cluster scaffold protein ISCU causes myopathy with exercise intolerance.

Authors:  Fanny Mochel; Melanie A Knight; Wing-Hang Tong; Dena Hernandez; Karen Ayyad; Tanja Taivassalo; Peter M Andersen; Andrew Singleton; Tracey A Rouault; Kenneth H Fischbeck; Ronald G Haller
Journal:  Am J Hum Genet       Date:  2008-02-14       Impact factor: 11.025

4.  Elevated FGF21 secretion, PGC-1α and ketogenic enzyme expression are hallmarks of iron-sulfur cluster depletion in human skeletal muscle.

Authors:  Daniel R Crooks; Thanemozhi G Natarajan; Suh Young Jeong; Chuming Chen; Sun Young Park; Hongzhan Huang; Manik C Ghosh; Wing-Hang Tong; Ronald G Haller; Cathy Wu; Tracey A Rouault
Journal:  Hum Mol Genet       Date:  2013-08-13       Impact factor: 6.150

5.  The High Level of Aberrant Splicing of ISCU in Slow-Twitch Muscle May Involve the Splicing Factor SRSF3.

Authors:  Denise F R Rawcliffe; Lennart Österman; Hans Lindsten; Monica Holmberg
Journal:  PLoS One       Date:  2016-10-26       Impact factor: 3.240

Review 6.  Iron-sulfur clusters: from metals through mitochondria biogenesis to disease.

Authors:  Mauricio Cardenas-Rodriguez; Afroditi Chatzi; Kostas Tokatlidis
Journal:  J Biol Inorg Chem       Date:  2018-03-06       Impact factor: 3.358

7.  FDX2 and ISCU Gene Variations Lead to Rhabdomyolysis With Distinct Severity and Iron Regulation.

Authors:  Sebastian Montealegre; Elise Lebigot; Hugo Debruge; Norma Romero; Bénédicte Héron; Pauline Gaignard; Antoine Legendre; Apolline Imbard; Stéphanie Gobin; Emmanuelle Lacène; Patrick Nusbaum; Arnaud Hubas; Isabelle Desguerre; Aude Servais; Pascal Laforêt; Peter van Endert; François Jérome Authier; Cyril Gitiaux; Pascale de Lonlay
Journal:  Neurol Genet       Date:  2022-01-19

8.  PTBP1 acts as a dominant repressor of the aberrant tissue-specific splicing of ISCU in hereditary myopathy with lactic acidosis.

Authors:  Denise F R Rawcliffe; Lennart Österman; Angelica Nordin; Monica Holmberg
Journal:  Mol Genet Genomic Med       Date:  2018-09-12       Impact factor: 2.183

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.