Literature DB >> 9061566

Severe lactic acidosis and neonatal death in Pearson syndrome.

K Muraki1, Y Goto, I Nishino, M Hayashidani, S Takeuchi, S Horai, N Sakura, K Ueda.   

Abstract

Pearson marrow-pancreas syndrome, a fatal disease associated with mitochondrial DNA rearrangements, is characterized by refractory sideroblastic anaemia during infancy. Only a few neonates with Pearson syndrome have been reported with metabolic acidosis. A female neonate who exhibited severe metabolic acidosis and anaemia at birth is described here. Her condition progressively worsened, with pancytopenia and uncontrollable metabolic acidosis resulting in death at the age of 14 days. A 4988-base pair deletion of mtDNA was detected in the patient's leukocytes, liver and muscle. When a neonate exhibits severe metabolic acidosis of unknown cause, the possibility of Pearson syndrome should be considered.

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Year:  1997        PMID: 9061566     DOI: 10.1023/a:1005305422544

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  13 in total

1.  Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy.

Authors:  A Rötig; V Cormier; S Blanche; J P Bonnefont; F Ledeist; N Romero; J Schmitz; P Rustin; A Fischer; J M Saudubray
Journal:  J Clin Invest       Date:  1990-11       Impact factor: 14.808

2.  Detection of DNA fragments encompassing the deletion junction of mitochondrial genome.

Authors:  Y Goto; I Nishino; S Horai; I Nonaka
Journal:  Biochem Biophys Res Commun       Date:  1996-05-15       Impact factor: 3.575

3.  Syndrome of refractory sideroblastic anemia with vacuolization of marrow precursors and exocrine pancreatic dysfunction presenting in the neonate.

Authors:  R A Stoddard; D C McCurnin; S J Shultenover; J E Wright; R A deLemos
Journal:  J Pediatr       Date:  1981-08       Impact factor: 4.406

4.  Mitochondrial diabetes revisited.

Authors:  S W Ballinger; J M Shoffner; S Gebhart; D A Koontz; D C Wallace
Journal:  Nat Genet       Date:  1994-08       Impact factor: 38.330

5.  Sequence and organization of the human mitochondrial genome.

Authors:  S Anderson; A T Bankier; B G Barrell; M H de Bruijn; A R Coulson; J Drouin; I C Eperon; D P Nierlich; B A Roe; F Sanger; P H Schreier; A J Smith; R Staden; I G Young
Journal:  Nature       Date:  1981-04-09       Impact factor: 49.962

6.  Site-specific deletions of the mitochondrial genome in the Pearson marrow-pancreas syndrome.

Authors:  A Rötig; V Cormier; F Koll; C E Mize; J M Saudubray; A Veerman; H A Pearson; A Munnich
Journal:  Genomics       Date:  1991-06       Impact factor: 5.736

7.  Molecular and genetic analyses of two patients with Pearson's marrow-pancreas syndrome.

Authors:  T Sano; K Ban; T Ichiki; M Kobayashi; M Tanaka; K Ohno; T Ozawa
Journal:  Pediatr Res       Date:  1993-07       Impact factor: 3.756

8.  Maternally inherited duplication of the mitochondrial genome in a syndrome of proximal tubulopathy, diabetes mellitus, and cerebellar ataxia.

Authors:  A Rötig; J L Bessis; N Romero; V Cormier; J M Saudubray; P Narcy; G Lenoir; P Rustin; A Munnich
Journal:  Am J Hum Genet       Date:  1992-02       Impact factor: 11.025

9.  Spectrum of mitochondrial DNA rearrangements in the Pearson marrow-pancreas syndrome.

Authors:  A Rötig; T Bourgeron; D Chretien; P Rustin; A Munnich
Journal:  Hum Mol Genet       Date:  1995-08       Impact factor: 6.150

10.  A new syndrome of refractory sideroblastic anemia with vacuolization of marrow precursors and exocrine pancreatic dysfunction.

Authors:  H A Pearson; J S Lobel; S A Kocoshis; J L Naiman; J Windmiller; A T Lammi; R Hoffman; J C Marsh
Journal:  J Pediatr       Date:  1979-12       Impact factor: 4.406

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  1 in total

1.  The association between haematological manifestation and mtDNA deletions in Pearson syndrome.

Authors:  K Muraki; S Nishimura; Y Goto; I Nonaka; N Sakura; K Ueda
Journal:  J Inherit Metab Dis       Date:  1997-09       Impact factor: 4.982

  1 in total

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