Abstract
Hereditary alpha-tryptasemia (HaT) is a common genetic condition with replication of the gene encoding for alpha tryptase. The HaT phenotype may be associated with dysautonomia and congenital connective tissue disorders, such as hypermobility spectrum disorder (HSD). We examined the association between HaT and abnormalities of collagen and elastin deposition on skin biopsies of patients with HaT.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
