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Miller, L

Congenital lactase deficiency or hereditary alactasia This is a rare disorder caused by a mutation in the LCT gene which results in the absence of lactase and hence the inability of affected infants to break down the lactose present in breastmilk or formula, this can lead to severe diarrhoea and subsequent dehydration and weight loss if lactose is not excluded 1,4

PMID:40074721

Im just saying, lets be careful in select patients because I think theres the potential to do harm," he added

Therefore, CJC-1295 no DAC may be best administered right before bed

However, genetic or medical reasons can cause some people produce too little