Disease #04245 (PEOA (ophthalmoplegia, external, progressive, with mitochondrial DNA deletions, autosomal dominant (PEOA)))

Official abbreviation PEOA
Name ophthalmoplegia, external, progressive, with mitochondrial DNA deletions, autosomal dominant (PEOA)
OMIM ID -
Inheritance -
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -
Date created 2015-05-01 19:52:34 +02:00 (CEST)
Date last edited N/A


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00046789 - PubMed: Reyes 2015, Journal: Reyes 2015 2-generation family, 1 affected,unaffected heterozygous carrier parents F no - - >42y - - - PEOA see paper; ... RNASEH1 RNASEH1 2 1 Johan den Dunnen
00046790 - PubMed: Reyes 2015, Journal: Reyes 2015 2-generation family, 1 affected, unaffected heterozygous carrier parents/sibs M no - - >46y - - - PEOA see paper; ... RNASEH1 RNASEH1 2 1 Johan den Dunnen
00046791 - PubMed: Reyes 2015, Journal: Reyes 2015, PubMed: Legati 2016 3-generation family, 4 affecteds (3F, 1M), unaffected heterozygous carrier parents/children F yes Italy - - - - - PEOA see paper; ..., progressive external ophtalmoparesis, cerebellar signs RNASEH1 RNASEH1 1 4 Johan den Dunnen
00387997 patient PubMed: Hedberg-Oldfors 2020 2-generation family, 1 affected, unaffected heterozygous carrier relatives M no Sweden - - - - - PEOA bilateral ptosis (HP:0001488), horizontal ophthalmoplegia (HP:0000602), slight bilateral sensory-neuronal hearing impairment (HP:0008619), atrophy of the mesencephalon pedunculus cerebelli superior (HP:0001272), frontotemporal parts of the brain (HP:0006892) POLG POLG 2 1 Giovanna Aschettino
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