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2. Fabry disease - Wikipedia

   en.wikipedia.org/wiki/Fabry_disease

   Fabry disease, also known as Anderson–Fabry disease, is a rare genetic disease that can affect many parts of the body, including the kidneys, heart, brain, and skin. [1] Fabry disease is one of a group of conditions known as lysosomal storage diseases .

3. 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.

4. Lipid storage disorder - Wikipedia

   en.wikipedia.org/wiki/Lipid_storage_disorder

   They are generally inherited in an autosomal recessive fashion, but Fabry disease is X-linked. Taken together, sphingolipidoses have an incidence of approximately 1 in 10,000. Enzyme replacement therapy is available mainly to treat Fabry disease and Gaucher disease and people with these types of sphingolipidoses may live well into adulthood ...

5. Sangamo's Fabry Disease Gene Therapy Continues To Show ... - AOL

   www.aol.com/news/sangamos-fabry-disease-gene...

   Sangamo Therapeutics Inc (NASDAQ: SGMO) has announced updated preliminary results from the Phase 1/2 STAAR study of isaralgagene civaparvovec, or ST-920, a gene therapy candidate for Fabry disease.

6. 4D Molecular Shares Updated Data From Fabry Disease Trial

   www.aol.com/news/4d-molecular-shares-updated...

   4D Molecular Therapeutics Inc (NASDAQ: FDMT) has posted updated interim data from the Phase 1/2 trial of 4D-310 in Fabry disease at the 18th Annual WORLDSymposium. Following 4D-310 infusion, mean ...

7. List of genetic disorders - Wikipedia

   en.wikipedia.org/wiki/List_of_genetic_disorders

   The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene" is common, it is the occurrence of an abnormality in the parents that causes the impairment to develop within the child.

8. 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.

9. Numerous factors can cause kidney disease. Here are the ... - AOL

   www.aol.com/numerous-factors-cause-kidney...

   AKI - the other main type of kidney disease - can be caused by dehydration, blood loss, urinary tract obstructions such as kidney stones or blood clots, low blood pressure, or heart disease. It ...