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Results 1 - 4 of 4 for Pearson syndrome
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  1. Mitochondrial DNA 
    ... syndrome (described above), deletion of mitochondrial DNA causes Pearson syndrome. This severe condition affects the development of blood ... lead to the specific signs and symptoms of Pearson syndrome.It is not clear why the same deletion ...
    https://medlineplus.gov/genetics/chromosome/mitochondrial-dna - Genetics
  2. Chromosome 17 
    ... Hunter JV, Sparagana S, Lagoe E, Fong CT, Pearson M, Doco-Fenzy M, Landais E, Mozelle M, Chinault AC, Patel A, Bacino CA, Sahoo T, Kang SH, Cheung SW, Lupski JR, Stankiewicz P. Microdeletions including YWHAE in the Miller-Dieker syndrome region on chromosome 17p13.3 result in facial ...
    https://medlineplus.gov/genetics/chromosome/17 - Genetics
  3. X chromosome 
    ... or Free article on PubMed Central Vallender EJ, Pearson NM, Lahn ... Jr. Klinefelter syndrome and other sex chromosomal aneuploidies. Orphanet J Rare ...
    https://medlineplus.gov/genetics/chromosome/x - Genetics
  4. Chromosome 1 
    ... in monosomy 1p36, and clinical characterization of the syndrome. Am J Hum Genet. 2003 May;72(5):1200-12. doi: 10.1086/375179. Epub 2003 Apr 8. Citation on PubMed or Free article on PubMed Central Ichimura K, Vogazianou AP, Liu L, Pearson DM, Backlund LM, Plant K, Baird K, Langford ...
    https://medlineplus.gov/genetics/chromosome/1 - Genetics