ODCs

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3 OMIM references -
3 associated genes
No signs/symptoms info

COMMON GENES: 1

1 OMIM reference -
3 associated genes
14 signs/symptoms

Mitochondrial neurogastrointestinal encephalomyopathy

Kearns-Sayre syndrome

Citations in the biomedical literature:

Mitochondrial neurogastrointestinal encephalomyopathy		Kearns-Sayre syndrome
	Synonym(s): - MNGIE		Synonym(s): (no synonyms)

	Classification (Orphanet): - Inborn errors of metabolism - Rare eye disease - Rare gastroenterologic disease - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare cardiac disease - Rare developmental defect during embryogenesis - Rare endocrine disease - Rare eye disease - Rare genetic disease - Rare neurologic disease - Rare otorhinolaryngologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the eye and adnexa -

	Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: adolescence / young Average age of death: adult Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: childhood Average age of death: young adult Type of inheritance: mitochondrial inheritance

	External references: 3 OMIM references - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D007625

Kearns-Sayre syndrome
	Very frequent - Cardiac conduction defect / sinoauricular / heart / auriculoventricular / branch block - Ophthalmoplegia / ophthalmoparesis / oculomotor palsy - Retinitis pigmentosa / retinal pigmentary changes Frequent - Abnormal EMG / electromyogram / electropmyography - Abnormal muscle biopsy / muscle enzymes / CPK / LDH / aldolase / creatin phosphokinase - Areflexia / hyporeflexia - Ataxia / incoordination / trouble of the equilibrium - Hearing loss / hypoacusia / deafness - Hypothalamic-hypophyseal axis functional anomalies / hypopituitarism - Hypotonia - Muscle hypotrophy / atrophy / dystrophy / agenesis / amyotrophy - Short stature / dwarfism / nanism Occasional - Delayed bone age - Hemiplegia / diplegia / hemiparesia / limb palsy
Mitochondrial neurogastrointestinal encephalomyopathy
(no data available)