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  2. Farber disease - Wikipedia

    en.wikipedia.org/wiki/Farber_disease

    Farber disease (also known as Farber's lipogranulomatosis, acid ceramidase deficiency, "Lipogranulomatosis", [2] and ASAH1-related disorders) is an extremely rare, progressive, autosomal recessive lysosomal storage disease caused by a deficiency of the acid ceramidase enzyme.

  3. List of diseases (F) - Wikipedia

    en.wikipedia.org/wiki/List_of_diseases_(F)

    This is a list of diseases starting with the letter "F". ... Farber's disease; Farmer's lung; ... Free sialic acid storage disease;

  4. List of human disease case fatality rates - Wikipedia

    en.wikipedia.org/wiki/List_of_human_disease_case...

    Human infectious diseases may be characterized by their case fatality rate (CFR), the proportion of people diagnosed with a disease who die from it (cf. mortality rate).It should not be confused with the infection fatality rate (IFR), the estimated proportion of people infected by a disease-causing agent, including asymptomatic and undiagnosed infections, who die from the disease.

  5. Sphingolipidoses - Wikipedia

    en.wikipedia.org/wiki/Sphingolipidoses

    Enzyme replacement therapy is available to treat mainly Fabry disease and Gaucher disease, and people with these types of sphingolipidoses may live well into adulthood. The other types are generally fatal by age 1 to 5 years for infantile forms, but progression may be mild for juvenile- or adult-onset forms.

  6. Lipid storage disorder - Wikipedia

    en.wikipedia.org/wiki/Lipid_storage_disorder

    Lipid storage diseases can be inherited two ways: Autosomal recessive inheritance occurs when both parents carry and pass on a copy of the faulty gene, but neither parent show signs and symptoms of the condition and is not affected by the disorder. Each child born to these parents have a 25 percent chance of inheriting both copies of the ...

  7. Metachromatic leukodystrophy - Wikipedia

    en.wikipedia.org/wiki/Metachromatic_leukodystrophy

    25% (1 in 4) of children will have the disease; 50% (2 in 4) of children will be carriers, but unaffected; 25% (1 in 4) children will be free of MLD – unaffected child that is not a carrier; If one parent is affected and one is free of MLD: 0% (0) children will have the disorder – only one parent is affected, other parent always gives ...

  8. Neuronal ceroid lipofuscinosis - Wikipedia

    en.wikipedia.org/wiki/Neuronal_ceroid_lipofuscinosis

    The classic characterization of the group of neurodegenerative, lysosomal storage disorders called the neuronal ceroid lipofuscinoses (NCLs) is through the progressive, permanent loss of motor and psychological ability with a severe intracellular accumulation of lipofuscins, [2] [3] with the United States and Northern European populations having slightly higher frequency with an occurrence of ...

  9. Sidney Farber - Wikipedia

    en.wikipedia.org/wiki/Sidney_Farber

    Sidney Farber (September 30, 1903 – March 30, 1973) was an American pediatric pathologist.He is regarded as the father of modern chemotherapy for his work using folic acid antagonists to combat leukemia, which led to the development of other chemotherapeutic agents against other malignancies.