Katafibrosis Syndrome
Katafibrosis Syndrome is a degenerative illness caused by unstable kata exposure over time. It is characterised by gradual degradation of the fibres in muscle and bone (depending on the type) as unstable kata is absorbed by the body's cells and causes muscle wasting and deformation of bone matter. It is one of a number of conditions caused by either being born in or living in one of the Amnari Exclusion Zones.
Katafibrosis is divided into a number of subtypes, the primary types (I, II, and III) being more severe and dangerous than forms IV, V, and VI. A seventh form, which may in fact be a separate condition affecting primarily collagen and connective tissue, is not degenerative but causes similar symptoms, including chronic pain of various kinds, as well as digestive, cognitive, and neurological problems, fatigue, and insomnia. Discussions around whether katafibrosis B, or Collagen and Connective Katafibrosis, should be considered an entirely separate syndrome, are ongoing.
The prognosis for Katafibrosis depends on subtype. Types I, II, and III may result in severe disability, included limited mobility, and rapid degeneration within two to three decades even with the best possible treatment and management of symptoms. Types IV and V can be managed more easily with regular treatment and full support, while Type VI patients can sometimes be expected to lead full and productive lives with appropriate full-time support from a dedicated team.
Treatment
Treatment depends on type. Screening is conducted for major internal differences resulting from exposure to unstable kata from the Gaps throughout the Amnari lifetime. Diagnosis therefore occurs rapidly and treatment plans can be put in place, to be altered depending on new information over time. All patients receive specialist assistance from a dedicated team of Watchers, led by a senior Watcher who provides one-to-one support and ongoing monitoring.
Type
Magical
Origin
Magical
Cycle
Chronic, Acquired & Congenital
Rarity
Common
Affected Species
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