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Up to: Lysosomal lipid storage disorder · Disorder of phospholipids, sphingolipids and fatty acids biosynthesis
Neutral lipid storage disease
Neutral lipid storage disease (NLSD) refers to a group of diseases characterized by a deficit in the degradation of cytoplasmic triglycerides and their accumulation in cytoplasmic lipid vacuoles in most tissues of the body. The group is heterogeneous: currently cases of NLSD with icthyosis (NLSDI/Dorfman-Chanarin disease) and NLSD with myopathy (NLSDM/neutral lipid storage myopathy) can be distinguished.
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Dorfman-Chanarin disease 1 trial
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Neutral lipid storage myopathy 0 trials