Kobayashi K

Kyowa Kirin (Japan)

1
Publications
35
h-index
(4,392 citations, 294 total works)

Research Topics

Clostridium difficile and Clostridium perfringens research (50) Metabolism and Genetic Disorders (38) Toxin Mechanisms and Immunotoxins (29) Streptococcal Infections and Treatments (22) Botulinum Toxin and Related Neurological Disorders (20)

PFAPA Syndrome Publications

Familial Mediterranean fever with P369S/R408Q exon3 variant in pyrin presenting as symptoms of PFAPA.

Yamagami K, Nakamura T, Nakamura R, Hanioka Y, Seki K , et al.
Modern rheumatology

Familial Mediterranean fever (FMF) can be classified into typical and incomplete/atypical types. Periodic fever, aphthous stomatitis, pharyngitis, cervical adenitis (PFAPA) syndrome-like symptoms have been found in atypical type carrying P369S-R408Q mutations in the responsible gene MEFV. A 28-year-old female with recurrent fever and her young sisters and mother, all of whom had tonsillectomy for tonsillitis, carried heterozygous alterations involving E148Q/P369S/R408Q. A diagnosis of atypical FMF, MEFV exon3 variants with PFAPA syndrome-like symptoms, was made.