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Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome

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Disease definition

Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome is a rare, genetic, neurodegenerative disease characterized by episodic metabolic encephalomyopathic crises (of variable frequency and severity which are frequently precipitated by an acute illness) which manifest with profound muscle weakness, ataxia, seizures, cardiac arrhythmias, rhabdomyolysis with myoglobinuria, elevated plasma creatine kinase, hypoglycemia, lactic acidosis, increased acylcarnitines and a disorientated or comatose state. Global developmental delay, intellectual disability and cortical, pyramidal and cerebellar signs develop with subsequent progressive neurodegeneration causing loss of expressive language and varying degrees of cerebral atrophy.

ORPHA:480864

Classification level: Disorder

Synonym(s):
  • TANGO2-related metabolic encephalopathy-arrhythmia syndrome

Source: PubMed ID 26805781 26805782

Prevalence: <1 / 1 000 000

Inheritance: Autosomal recessive

Age of onset: Infancy

ICD-10: G31.8

ICD-11: 8E4Y

OMIM: 616878

UMLS: C5567524

GARD: 13423

A summary on this disease is available in Français, Español, Deutsch, Italiano, Nederlands
Detailed information

Logo ERN: produced/endorsed by ERN(s) Logo FSMR: produced/endorsed by FSMR(s)

Guidelines
Emergency guidelines
Disease review articles
Clinical genetics review
English (2023) - GeneReviews
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