HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Waldmann disease

A rare disorder characterized by dilated intestinal lacteals that cause lymph leakage into the small bowel lumen, resulting in PROTEIN-LOSING ENTEROPATHIES and lower limb EDEMA. Onset is usually before 3 years of age but it may be diagnosed in older patients.
Also Known As:
Familial Waldmann's disease; Primary intestinal lymphangiectasis; Waldmann's disease
Networked: 8 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Related Diseases

1. Necrolytic Migratory Erythema
2. Lymphatic Abnormalities
3. Intestinal Diseases (Diseases, Intestinal)
4. Agammaglobulinemia (Hypogammaglobulinemia)

Experts

1. Aryal, Nirjala: 1 article (06/2022)
2. Bohara, Sujan: 1 article (06/2022)
3. Karki, Samikshya: 1 article (06/2022)
4. Mainali, Gaurab: 1 article (06/2022)
5. Prajapati, Sarita: 1 article (06/2022)
6. Thapa, Sharan: 1 article (06/2022)
7. Babakhouya, Abdeladim: 1 article (08/2021)
8. Benajiba, Noufissa: 1 article (08/2021)
9. El Haddar, Zohair: 1 article (08/2021)
10. Rkain, Maria: 1 article (08/2021)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Waldmann disease:
1. Proteins (Proteins, Gene)FDA Link
2. Octreotide (Sandostatin)FDA LinkGeneric
3. Triglycerides (Triacylglycerol)IBA
4. Immunoglobulins (Immunoglobulin)IBA
5. Fatty Acids (Saturated Fatty Acids)IBA
6. Complement System Proteins (Complement)IBA
7. Blood Proteins (Serum Proteins)IBA
8. Amino AcidsFDA Link

Therapies and Procedures

1. Therapeutics
2. High-Protein Diet