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Acid lipase disease or deficiency is a name used to describe two related disorders of fatty acid metabolism. Acid lipase disease occurs when the enzyme lysosomal acid lipase that is needed to break down certain fats that are normally digested by the body is lacking or missing. This results in the toxic buildup of these fats in the body's cells ...
Lysosomal acid lipase deficiencies occur when a person has defects (mutations) in both copies of the LIPA gene. Each parent of a person with LAL deficiency carries one copy of the defective LIPA gene. With every pregnancy, parents with a son or daughter affected by LAL deficiency have a 1 in 4 (25%) chance of having another affected child.
Alopecia Areata. Alopecia areata is an autoimmune condition that affects about 2 percent of the population. It occurs when your immune system attacks your hair follicles. This can damage your ...
Traction alopecia. Constant tension or strain on the hair damages the follicle, impacting the ability for blood flow and nutrients to reach it and can ultimately result in permanent hair loss, Dr ...
A review of studies found that people with certain autoimmune diseases may have a vitamin D deficiency. ... Alopecia areata and the patchy hair loss it causes can be distressing. Plus, because ...
The cause of male-pattern hair loss is a combination of genetics and male hormones; the cause of female pattern hair loss is unclear; the cause of alopecia areata is autoimmune; and the cause of telogen effluvium is typically a physically or psychologically stressful event. [4] Telogen effluvium is very common following pregnancy. [4]
Women's hair loss can be caused by many factors, from alopecia to pregnancy to poor diet. Here, doctors discuss how to prevent hair loss and the best regrowth treatments. ... Here, doctors discuss ...
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.