A rare mutation causing autosomal dominant STAT1 deficiency in a South African multiplex kindred with disseminated BCG infection.

Leonore GreybeDaniel LeungNicole WieselthalerDavid M le RouxKoon Wing ChanYu Lung LauBrian Eley

Published in: BMC pediatrics (2023)

Children with BCG vaccine complications in SSA should be referred for further investigation and particular consideration of MSMD.

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