GAF
Member
Wolman disease is a rare genetic disorder characterized by complete absence of the lysosomal acid lipase enzyme. It is often fatal within the first six months of life. Without the LIPA enzyme, certain lipids may abnormally accumulate in the tissues and organs of the body causing a variety of symptoms.
CESD is the later onset of wolmans and it's not rare, it's the common cause of hardening of arteries. It's the lack of LAL enzyme... pancreas issue...
CESD is the later onset of wolmans and it's not rare, it's the common cause of hardening of arteries. It's the lack of LAL enzyme... pancreas issue...