- Congenital muscular dystrophy with integrin alpha-7 deficiency
- Congenital muscular dystrophy with ITGA7 deficiency
- Intestinal lipodystrophy
- Intestinal lipophagic granulomatosis
- Secondary Non-tropical Sprue
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Depending on the seriousness of the disease, treatment may also include fluid and electrolyte replacement. Electrolytes are salts and other substances in body fluid that the heart and brain need to function properly. Extra iron, folate, vitamin D, calcium, and magnesium may also be given to help compensate for the vitamins and minerals the body cannot absorb on its own.
Individuals who are being treated for Whipple disease should be closely monitored by a health care provider because signs of the disease can return after therapy has been finished. Full recovery of the small intestine may take up to 2 years, but the symptoms usually disappear in less time. Because relapse is common even after successful treatment, the health care team may continue to monitor the patient for many years.
- NINDS Whipple's Disease Information Page. National Institute of Neurological Disorders and Stroke (NINDS). March 22, 2011; http://www.ninds.nih.gov/disorders/whipples/whipples.htm. Accessed 8/1/2012.
- Whipple's Disease. National Digestive Diseases Information Clearinghouse (NDDIC). April 30, 2012; http://digestive.niddk.nih.gov/ddiseases/pubs/whipple/index.htm. Accessed 8/1/2012.
- Dugdale DC, Longstreth GF. Whipple's disease. MedlinePlus. May 1, 2012; http://www.nlm.nih.gov/medlineplus/ency/article/000209.htm. Accessed 8/1/2012.