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    Inflammatory Bowel Disease Health Center

    Medical Reference Related to Inflammatory Bowel Disease

    1. Niemann Pick Disease Type C

      Niemann-Pick disease (NPD) is a group of rare inherited disorders of fat metabolism. At least five types of Niemann-Pick disease have been identified (NPD types A,B,C,D,and E). Symptoms of types A and B occur as a result of a deficiency of the enzyme acid sphingomyelinase (ASM),which is needed to break down sphingomyelin,a fatty substance found mostly in the brain and nervous system. ...

    2. Leukodystrophy, Metachromatic

      Important It is possible that the main title of the report Leukodystrophy, Metachromatic is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. ...

    3. Distal Myopathy

      Distal myopathy (or distal muscular dystrophy) is a general term for a group of rare progressive genetic disorders characterized by wasting (atrophy) and weakness of the voluntary distal muscles. The distal muscles are those farther from the center of the body and include the muscles of the lower arms and legs and the hands and feet. Conversely,the proximal muscles are the muscles closest to ...

    4. Empty Sella Syndrome

      Important It is possible that the main title of the report Empty Sella Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. ...

    5. Leukodystrophy, Krabbe's

      Important It is possible that the main title of the report Leukodystrophy, Krabbe's is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. ...

    6. Sandhoff Disease

      Sandhoff disease is a lipid storage disorder characterized by a progressive deterioration of the central nervous system. The clinical symptoms of Sandhoff disease are identical to Tay-Sachs disease. Sandhoff disease is an autosomal recessive genetic disorder caused by an abnormal gene for the beta subunit of the hexosaminidase B enzyme. This gene abnormality results in a deficiency of ...

    7. Reflex Sympathetic Dystrophy Syndrome

      Important It is possible that the main title of the report Reflex Sympathetic Dystrophy Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. ...

    8. Idiopathic Intracranial Hypertension

      Important It is possible that the main title of the report Pseudotumor Cerebri is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. ...

    9. Cervical Dystonia

      Important It is possible that the main title of the report Spasmodic Torticollis is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. ...

    10. Bell's Palsy

      Bell's palsy is a nonprogressive neurological disorder of one of the facial nerves (7th cranial nerve). This disorder is characterized by the sudden onset of facial paralysis that may be preceded by a slight fever,pain behind the ear on the affected side,a stiff neck,and weakness and/or stiffness on one side of the face. Paralysis results from decreased blood supply (ischemia) and/or ...

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