Understanding Congenital Myasthenic Syndrome disease
Congenital Myasthenic Syndrome, also known as congenital myasthenia, is related to myasthenic syndrome, congenital, 4c, associated with acetylcholine receptor deficiency and myasthenic syndrome, congenital, 5, and has symptoms including facial paresis An important gene associated with Congenital Myasthenic Syndrome is CHRNE (Cholinergic ...
Christianson Syndrome: A Rare Genetic Disorder disease
Christianson Syndrome, also known as x-linked angelman-like syndrome, is related to angelman syndrome and complex partial epilepsy, and has symptoms including ataxia, ophthalmoplegia and sleep disturbances. An important gene associated with Christianson Syndrome is SLC9A6 (Solute Carrier Family 9 Member A6), and among its related ...
Managing Cold Agglutinin Disease: A Wellness Approach disease
Cold Agglutinin Disease, also known as chronic cold agglutinin disease, is related to autoimmune hemolytic anemia, cold type and warm antibody hemolytic anemia. The drugs Agglutinins and Pharmaceutical Solutions have been mentioned in the context of this disorder. Affiliated tissues include bone marrow, bone and neutrophil, and related ...
Living with DIC: Managing Lifestyle and Health disease
Disseminated Intravascular Coagulation, also known as defibrination syndrome, is related to dic in newborn and purpura fulminans. An important gene associated with Disseminated Intravascular Coagulation is SERPINC1 (Serpin Family C Member 1), and among its related pathways/superpathways are Response to elevated platelet cytosolic Ca2+ and ...
Understanding Bainbridge-Ropers Syndrome disease
Bainbridge-Ropers Syndrome, also known as severe feeding difficulties-failure to thrive-microcephaly due to asxl3 deficiency syndrome, is related to bohring-opitz syndrome and microcephaly. An important gene associated with Bainbridge-Ropers Syndrome is ASXL3 (ASXL Transcriptional Regulator 3), and among its related pathways/superpathways ...