Orphanet: Adult onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency

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Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency

Disease definition

An extremely rare multiple mitochondrial DNA deletion syndrome with markedly decreased deoxyguanosine kinase (DGUOK) activity in skeletal muscle characterized by a highly variable phenotype. Clinical manifestations include progressive external ophthalmoplegia, mitochondrial myopathy, recurrent rhabdomyolysis, lower motor neuron disease, mild cognitive impairment, sensory axonal neuropathy, optic atrophy, ataxia, hypogonadism and/or parkinsonism.

ORPHA:329314

Classification level: Disorder

Synonym(s):
- Adult-onset multiple mtDNA deletion syndrome due to DGUOK deficiency
Prevalence: Unknown
Inheritance: Autosomal recessive
Age of onset: Adult
ICD-10: G71.3
OMIM: 617070
UMLS: -
MeSH: -
GARD: -
MedDRA: -

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Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency

ORPHA:329314

A summary on this disease is available in Deutsch (2017) Español (2017) Français (2017) Italiano (2017) Nederlands (2017)

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