toIPA
Home
Blog
Category
Pfeiffer syndrome
acrocephalosyndactylia that has material basis in mutations in the FGFR1 and FGFR2 gene which results in premature fusion located in skull
Pronunciation
/ˈfaɪfər ˈsɪnˌdroʊm/
Categories
acrocephalosyndactylia
genetic disease
rare disease