Article
Novel Mutations in CRLF1: Case Reports with Crisponi Syndrome.
Indian journal of pediatrics - 1 Nov 2022
A Rekha, Chandran Shanu, Ghatak Arpita Roy, Thomas Niranjan, Danda Sumita
Abstract excerpt
Crisponi syndrome (CS) is a rare autosomal recessive syndrome, characterized by episodic facial muscle contraction with trismus, abundant salivation along with intermittent hyperthermia, feeding difficulties, characteristic facial dysmorphism, and camptodactyly. Here the authors report two South Indian neonates with confirmed diagnosis of Crisponi syndrome, caused by novel pathogenic variants in cytokine...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
