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& Hamzakoya, K

X-linked recessive: 5 defects which are X-linked- CHO (G6PD deficiency) Lipid metabolism (Fabry's disease, caused by Alpha Galactosidase, which is X-linked recessively inherited) Amino acid metabolism (Type 2 Hyperammonemia) Puri Salvage metabolism- GPRTase defect, which is an enzyme of the Purine Salvage pathway, and the Defect of this enzyme causes Lesch Nyhan Syndrome

71,533,601,602,603,604 Morphological atrophy of astrocytes develops in a brain-region-linked fashion, starting first in the entorhinal and prefrontal cortices (which are, incidentally, the most vulnerable to AD) and then spreading to hippocampus

Key Points Statinfibrate combination regimens might be useful for patients with insulin resistance and certain types of dyslipidemia

This can be achieved through a combination of dietary sources (such as leafy green vegetables and fortified foods) and supplements