Autosomal recessive il12rb1 mutation: a case report of a sudanese child and his father

HIGHLIGHTS

• who: Omaima Abdelmajeed and colleagues from the The University of Hong Kong, Hong Kong SAR, China have published the paper: Autosomal recessive IL12RB1 mutation: A case report of a Sudanese child and his father, in the Journal: (JOURNAL)
• what: Diagnosing IL12RB1 mutations should be considered in patients with recurrent, severe, or persistent TB infection especially after obtaining the BCG vaccination.

SUMMARY

Mendelian susceptibility to mycobacterial disease (MSMD) is a rare inherited condition characterized by selective susceptibility to weakly virulent mycobacteria, such as substrains of the bacille Calmette-Gué rin (BCG) vaccine . . .

 



If you want to have access to all the content you need to log in!

Thanks :)

Username or Email

Password

Remember me

Lost your password?

If you don't have an account, you can create one here.