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In newborn screenings where biochemical markers are indicative of vitamin B 12 deficiency, the diagnosis of inborn errors of vitamin B 12 metabolism is performed via functional studies on cultured fibroblasts isolated from skin biopsies (Watkins and Rosenblatt, 2013) or via molecular genetic analysis of putative genes

Other rare symptoms may include irritability, microcephaly, autism spectrum disorder, tremor, global developmental delay, coma, polyneuropathy, axial hypotonia, and daytime sleepiness [100, 102,103,104,105,106,107,108]

It changes how the body stores and metabolizes fat at a hormonal level

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Whether it's a virtual consultation or an in-person visit with an IBCLC breastfeeding help consultation, getting expert eyes on your specific situation can make a world of difference