NR5A1 and adrenoleukodystrophy: Other genetic etiologies of non-CAH are adrenal gland developmental disorders [X-linked adrenal hypoplasia congenital (AHC), steroidogenic factor-1 related and other syndromic causes], ACTH resistance including familial GC deficiency (FGD) and related conditions and Triple A syndrome (TAS), metabolic causes [cholesterol synthesis/metabolism defects, adrenoleukodystrophy (ALD), other defects of the peroxisome, lysosome, endoplasmic reticulum and mitochondria], GC resistance and aldosterone synthesis/action defects (7,8).