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SPCD (OMIM 212140) is a rare autosomal recessive disorder, caused by homozygous or compound heterozygous mutation in the SLC22A5 gene

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Compounded formulations offer pharmacy flexibility and cost alternatives

Recognizing this distinction is essential to avoid over-pathologizing aging itself and to appropriately contextualize chronobiological and nutritional interventions as strategies for supporting functional resilience rather than reversing aging

The event served as a platform for exchanging perspectives on filler injection programs, along with updates on aesthetic directions in the Asia-Pacific region

The details provided here are not a replacement for, and should never be depended upon as, professional medical advice