Search

everythingexperts & clinicslearnfaqsresearchcommunity

for

Search:↓

The study suggests that integrin β1 is crucial for maintaining liver microstructure and its absence may promote fibrosis by disrupting hepatocyte-extracellular matrix interactions and increasing TGF-β secretion.

This study reports the discovery of mutations in the PADI3, TGM3, and TCHH genes as molecular genetic causes of uncombable hair syndrome in children, indicating an autosomal-recessive inheritance pattern.

Hair shaft changes may be linked to CCCA, but their role is unclear.

This paper discusses the use of dermatoscopy as a fast, noninvasive technique for diagnosing hair shaft disorders and reports no new results; the authors highlight its advantages over traditional microscopy methods.

Reduced androgens linked to kinky hair disorder and hair loss; 5a-reductase inhibitors may help.