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2,511 Possible Causes for Sache

  • Tuberculosis

    In order to raise public awareness, the Visiting Nurses Association and physician Theodore Sachs spearheaded an antituberculosis movement in the early 1900s.[]

  • Optic Atrophy

    Retinal storage diseases (eg, Tay-Sachs disease ). Radiation neuropathy. Syphilis .[] Congenital: Tay-Sachs, Retinitis Pigmentosa, Leber’s optic neuropathy, Friedreich’s ataxia.[]

  • Dementia

    ., Sachs G., Crabtree B., Keo R., Perez E.K., Taber S., Gilchrist J., Andoin A., Darnell T., Goyal N., Sakamuri S., So Y.T., Welsh L.W., Bhavaraju-Sanka R., Tobon Gonzalez[] Balaguer P., Osei-Bonsu M., Pan E.B.L., Pardo Fernandez J., Pasnoor M., Pulley M.T., Rajabally Y.A., Rinaldi S., Ritter C., Roberts R.C., Rojas-Marcos I., Rudnicki S.A., Sachs[]

  • Sandhoff's Disease

    Abstract In Tay-Sachs disease and Sandhoff's disease respectively, one of the N-acetyl-beta-hexosaminidases (form A) or both (forms A and B) are absent, but glycosaminoglycans[] As with Tay-Sachs disease the severity of Sandhoff disease depends on the amount of residual enzyme that is produced.[] Condition or disease Intervention/treatment Phase Gangliosidoses, GM2 Sandhoff Disease Tay-Sachs Disease Drug: Pyrimethamine Drug: Leucovorin Phase 1 Phase 2 Detailed Description[]

  • First Trimester Pregnancy

    Blood screening tests--to detect diseases (i.e., rubella, also called German measles) Genetic tests--to detect inherited diseases (i.e., sickle-cell anemia, Tay-Sachs disease[] […] paternal family medical history, including illnesses, such as diabetes or intellectual or developmental disabilities, and genetic disorders, like sickle cell disease or Tay-Sachs[] […] surgeries Maternal and paternal family medical history, including illnesses such as diabetes or mental retardation, and genetic disorders, such as sickle cell disease or Tay-Sachs[]

  • Late-onset Depression

    This condition is a recently discovered form of Tay-Sachs disease and occurs most often in people of Ashkenazi Jewish descent.[] Treatment for late-onset Tay-Sachs disease focuses on controlling symptoms. There is no cure. The life expectancy for a person with LOTS is unknown.[] Late-onset Tay-Sachs (LOTS) is a very rare genetic disease in which fatty compounds, called gangliosides, do not break down fully because the body produces too little of the[]

  • Amyotrophic Lateral Sclerosis

    […] include: Multifocal motor neuropathy, cervical myelopathy with radiculopathy, benign fasciculation syndrome, post-polio syndrome, spinobulbar muscular atrophy, late onset Tay-Sachs[] disease, paraneoplastic and autoimmune motor neuropathies, etc.[]

  • Adolescence

    [email protected] 4 Sachs' Children and Youth Hospital, The South General Hospital, 118 83 Stockholm, Sweden.[] Do not show again Brad Sachs says the nature of adolescence is timeless—and that’s a very good thing for the human race April 26, 2015 11:25 p.m.[] [email protected] 6 Institute for Environmental Medicine, Karolinska Institutet, 171 11 Stockholm, Sweden. [email protected] 7 Sachs' Children and Youth Hospital,[]

  • Neonatal Adrenoleukodystrophy

    Hydroxylase Deficiency Fucosidosis Fukuyama Congential Muscular Dystrophy Galactosialidosis Globoid Cell Leukodystrophy (Krabbe Disease) GM1 Gangliosidosis GM2 Gangliosidosis (Tay-Sachs[] Disease) Hereditary Adult Onset Leukodystrophy Simulating Chronic Progressive Multiple Sclerosis Herditary Diffuse Leukoencephalopathy with Axonal Spheroids (HDLS) Hypomyelination[]

  • GM2 Gangliosidosis Variant AB

    Pagina 9 - Sachs, B. : On arrested cerebral development, with special reference to its cortical pathology. ‎[] Página 9 - Sachs, B. : On arrested cerebral development, with special reference to its cortical pathology. ‎[] Clinical variant of Tay-Sachs disease or a new disease?[]

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