Disease #05147 (CPEO (ophthalmoplegia, external, progressive, chronic (CPEO)))

Official abbreviation CPEO
Name ophthalmoplegia, external, progressive, chronic (CPEO)
OMIM ID -
Inheritance -
Individuals reported having this disease 7
Phenotype entries for this disease 6
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -
Date created 2016-03-27 15:38:04 +02:00 (CEST)
Date last edited N/A


Individuals

7 entries on 1 page. Showing entries 1 - 7.
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00037297 - - - - - Germany - - - - - CPEO CPEO C10orf2 C10orf2 1 1 Andreas Laner
00037299 - - - - - Germany - - - - - CPEO CPEO C10orf2 C10orf2 1 1 Andreas Laner
00207382 - - also has a dominant MYH7 mutation with cardiomyopathy F no Portugal white >52y - - ubiquinone 200 mg daily CPEO - POLG POLG 3 3 André Militão
00276004 - - - ? ? Spain - - - - - CPEO - TMEM259 - - 1 Pablo Serrano-Lorenzo
00331302 - - - F yes India - - - - - CPEO - - C1QBP 1 1 Le Guo
00384650 patient PubMed: Lin 2021 2-generation family, 1 affected, unaffected heterozygous carrier mother M no China - - - - - CPEO strabismus (HP:0000486), ophthalmoplegia (HP:0000602), bilateral ptosis (HP:0001488), exotropia ( HP:0000577), ophthalmoparesis ( HP:0000597), Abnormality of eye movement ( HP:0000496) - POLG 2 1 Giovanna Aschettino
00443912 - - unaffected heterozygous carrier parents F no Brazil latin american - - - none CPEO ptosis (HP:0000508), Respiratory insufficiency due to muscle weakness (HP:0002747); Global developmental delay(HP:0001263); Hypotonia (HP:0001252) ;Weakness of facial musculature(HP:0030319); Ophthalmoparesis (HP:0000597); High palate (HP:0000218 - SURF1 2 1 Beatriz Betini
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