Skip to content
Use your HSA or FSA funds

Condition report · Neurological

Periodic Paralysis

A hereditary disorder characterized by recurrent episodes of muscle weakness or paralysis.

A condition report looks for rare variants known to cause the conditions it covers.

Included in Premium and Premium + AI

Premium adds $99 per kit for the first year.

Order with Premium

The condition we analyse

Periodic Paralysis

Autosomal dominant

Editor note: classified as genetic in ORDO but we treat as neutral here

Genes analysed

Also known as

periodic paralysis (disease)

Includes 9 related subtypes ↓
  • Andersen-Tawil syndrome
  • familial periodic paralysis
  • hyperkalemic periodic paralysis
  • hypokalemic periodic paralysis
  • hypokalemic periodic paralysis, type 1
  • hypokalemic periodic paralysis, type 2
  • normokalemic periodic paralysis
  • periodic paralysis with later-onset distal motor neuropathy
  • thyrotoxic periodic paralysis
MONDO:0016122Orphanet 206976MedGen 488958

Other neurological conditions

All conditions →

One test. A lifetime of answers.

One kit, sent to your home. Your entire genome sequenced at the clinical standard used for diagnostic decisions. Physician-ready reports delivered to your Genome Manager in 6–8 weeks — permanent and updated as science advances.

From $449

Free shipping · Results in 6–8 weeks

Premium adds $99 per kit for the first year.

Order with Premium