Ads
related to: rare chronic diseases- See the FAQs
Get the Answers to Frequently
Asked Questions Today.
- Join the Support Program
View Resources & Copay Assistance.
Terms & Conditions Apply.
- Talk to Your Doctor
Download the Discussion Guide
to Start the Conversation Today.
- View T1D Organizations
Stay Connected. Learn About
T1D Organizations Today.
- See the FAQs
Search results
Results From The WOW.Com Content Network
Chronic genetic diseases are commonly classified as rare. [ 20 ] [ 21 ] Among numerous possibilities, rare diseases may result from bacterial or viral infections, allergies , chromosome disorders, degenerative and proliferative causes, affecting any body organ . [ 20 ]
A rare disease is technically defined (in the European Union) as a disease that is found in fewer than 5 people per every 10,000 people. ...
This article provides a list of autoimmune diseases. These conditions, where the body's immune system mistakenly attacks its own cells, affect a range of organs and systems within the body. Each disorder is listed with the primary organ or body part that it affects and the associated autoantibodies that are typically found in people diagnosed ...
As with any disease, whether it's rare or common like high blood pressure, knowledge brings awareness that can be life-altering. The insights on these 10 rare diseases will help you improve your ...
Localized disease, a disease affecting one body part or area. Non-communicable disease, a disease that can not be spread between people. Organic disease; Progressive disease, a disease that gets worse over time. Rare disease, a disease that affects very few people. Systemic disease, a disease affecting the whole body.
Fatal insomnia is an extremely rare neurodegenerative prion disease that results in trouble sleeping as its hallmark symptom. [2] The majority of cases are familial (fatal familial insomnia [FFI]), stemming from a mutation in the PRNP gene, with the remainder of cases occurring sporadically (sporadic fatal insomnia [sFI]).
Pemphigus vulgaris is a rare chronic blistering skin disease and the most common form of pemphigus.Pemphigus was derived from the Greek word pemphix, meaning blister. [1] It is classified as a type II hypersensitivity reaction in which antibodies are formed against desmosomes, components of the skin that function to keep certain layers of skin bound to each other.
The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene" is common, it is the occurrence of an abnormality in the parents that causes the impairment to develop within the child.