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Liu J, Yin F, Zheng X, Jing J, Hu Y

Supplementary Table 11 presents the treatment outcomes for the single and double dental pulp stem cell injection groups and the saline control group

MKRN3 deficiency has been identified as a common genetic cause of CPP, with different prevalence rates in sporadic (0.5-17-5%) versus familial (9-46%) cases (212, 213)

457 Similarly post-mortem analysis revealed decreased levels of astrocytic EAAT1/2 glutamate transporters

When this barrier becomes damaged through excessive cleansing, harsh treatments, or environmental exposure, the skin becomes more susceptible to inflammation and reactive hyperpigmentation

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