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  2. Glycogen storage disease - Wikipedia

    en.wikipedia.org/wiki/Glycogen_storage_disease

    A glycogen storage disease(GSD, also glycogenosisand dextrinosis) is a metabolic disordercaused by a deficiency of an enzymeor transport proteinaffecting glycogen synthesis, glycogen breakdown, or glucose breakdown, typically in musclesand/or livercells. [1] GSD has two classes of cause: genetic and environmental.

  3. What happens to your medical debt after you die? - AOL

    www.aol.com/finance/what-happens-to-medical-debt...

    Assets you bought during marriage using separate property funds — such as a car purchased with money you earned before you married Gifts given to an individual spouse, since this is an unearned ...

  4. What happens if your life insurance beneficiary dies ... - AOL

    www.aol.com/finance/happens-life-insurance...

    For example, if you have three primary beneficiaries and one dies, the remaining two would likely split the death benefit equally. Paying the deceased beneficiary’s heirs: In some cases, the ...

  5. Glycogen storage disease type I - Wikipedia

    en.wikipedia.org/wiki/Glycogen_storage_disease...

    Glycogen storage disease type I (GSD I) is an inherited disease that prevents the liver from properly breaking down stored glycogen, which is necessary to maintain adequate blood sugar levels. GSD I is divided into two main types, GSD Ia and GSD Ib, which differ in cause, presentation, and treatment. There are also possibly rarer subtypes, the ...

  6. Glycogen storage disease type II - Wikipedia

    en.wikipedia.org/wiki/Glycogen_storage_disease...

    Endocrinology. Glycogen storage disease type II(GSD-II), also called Pompe disease, and formerly known as GSD-IIa or Limb–girdle muscular dystrophy 2V, is an autosomal recessive metabolic disorder [ 1 ] which damages muscle and nerve cells throughout the body.

  7. Glycogen storage disease type V - Wikipedia

    en.wikipedia.org/wiki/Glycogen_storage_disease...

    Glycogen storage disease type V (GSD5, GSD-V), [ 1 ] also known as McArdle's disease, [ 2 ] is a metabolic disorder, one of the metabolic myopathies, more specifically a muscle glycogen storage disease, caused by a deficiency of myophosphorylase. [ 3 ][ 4 ] Its incidence is reported as one in 100,000, roughly the same as glycogen storage ...

  8. How to protect your deceased loved one’s credit after death

    www.aol.com/finance/protect-deceased-loved-one...

    The bottom line. Protecting your deceased loved one’s credit report is helpful when you’re wrapping up their financial affairs. Start by notifying the credit bureaus of their passing, then ...

  9. Glycogen storage disease type III - Wikipedia

    en.wikipedia.org/wiki/Glycogen_storage_disease...

    gsd iii is ar In regards to genetics glycogen storage disease type III is inherited in an autosomal recessive pattern (which means both parents need be a carrier), and occurs in about 1 of every 100,000 live births.