Ad
related to: waldman's disease prognosis symptoms and signs- Signs of VOD Progression
Symptoms of multi-organ dysfunction
may be predictive of VOD/SOS
- Identifying VOD
Visit HCP site to learn how to
help identify progressive VOD.
- Risk Factors
Read about the preexisting factors
that may increase risk of VOD.
- Download VOD Resources
View resources that can
help identify and manage VOD.
- VOD Progression
Visit HCP site and learn
how to help identify VOD.
- VOD Incidence
View prevalence data
on VOD incidence.
- Signs of VOD Progression
Search results
Results From The WOW.Com Content Network
Signs and symptoms of the disease include diarrhea, nausea, swelling of the legs, protein-losing enteropathy, immunodeficiency and loss of lymphatic fluid into the intestines. [2] [4] It is usually diagnosed before the patient is 3 years old, but it is sometimes diagnosed in adults. [3]
Lymphangiectasia, also known as "lymphangiectasis", [1] is a pathologic dilation of lymph vessels. [2] When it occurs in the intestines it is known as intestinal lymphangiectasia, colloquially recognized as Waldmann's disease in cases where there is no secondary cause. [3]
Features relating to lung and liver disease may occur. [1] [5] It is due to a genetic mutation in the MAPKinase pathway that occurs during early development. [1] The diagnosis may be suspected based on symptoms and MRI and confirmed by tissue biopsy. [6] [7] Blood tests may show anaemia, and less commonly a low white blood cell count and low ...
Other features of the disease include a tendency toward leukocytosis, blood clot formation, abnormal lung function (restrictive lung disease, pulmonary hypertension, and impaired lung diffusion capacity), very high blood levels of the cytokine vascular endothelial growth factor (VEGF), and an overlap with the signs and symptoms of multicentric ...
Treatment is highly individualized and depends on a range of factors, including the subtype of the disease, its stage, the patient's age, and other medical conditions. [17] Patients with early-stage indolent lymphoma may be cured with radiation therapy, but most patients have widespread disease at the time of diagnosis. There are many effective ...
Treatment of Wiskott–Aldrich syndrome depends on the severity of the disease. WAS is primarily a disorder of the blood-forming tissues, so in cases of severe disease (WAS score 3–5) the only widely available curative treatment currently available is a hematopoietic stem cell transplant (HCT).
In 1986 Poser tried to restrict the use of Schilder's disease name to the disease described here, but this name has still remained ambiguous. [citation needed] The name comes from a traditional classification of demyelinating diseases in two groups: demyelinating myelinoclastic diseases and demyelinating leukodystrophic diseases. In the first ...
Hoffmann syndrome is a rare form of hypothyroid myopathy and is not to be confused with Werdnig-Hoffmann disease (a type of spinal muscular atrophy). It was first documented in 1897 by Johann Hoffmann. [1] It has adult-onset symptoms and is comparable to the childhood-onset Kocher–Debré–Semelaigne syndrome.