Pearson marrow-pancreas syndrome is a severe disorder that usually begins in infancy.
genetic conditions
References
Manea EM, Leverger G, Bellmann F, Stanescu PA, Mircea A, Lèbre AS, Rötig A,Munnich A. Pearson syndrome in the neonatal period: two case reports and reviewof the literature. J Pediatr Hematol Oncol. 2009 Dec;31(12):947-51. doi:10.1097/MPH.0b013e3181bbc4ef. Review.
Rötig A, Bourgeron T, Chretien D, Rustin P, Munnich A. Spectrum ofmitochondrial DNA rearrangements in the Pearson marrow-pancreas syndrome. Hum MolGenet. 1995 Aug;4(8):1327-30.
Sadikovic B, Wang J, El-Hattab AW, Landsverk M, Douglas G, Brundage EK,Craigen WJ, Schmitt ES, Wong LJ. Sequence homology at the breakpoint and clinicalphenotype of mitochondrial DNA deletion syndromes. PLoS One. 2010 Dec20;5(12):e15687. doi: 10.1371/journal.pone.0015687. Erratum in: PLoS One. 2017Nov 20;12 (11):e0188610.
Tumino M, Meli C, Farruggia P, La Spina M, Faraci M, Castana C, Di Raimondo V,Alfano M, Pittalà A, Lo Nigro L, Russo G, Di Cataldo A. Clinical manifestationsand management of four children with Pearson syndrome. Am J Med Genet A. 2011Dec;155A(12):3063-6. doi: 10.1002/ajmg.a.34288.
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