Familial case of Blau syndrome associated with a CARD15/NOD2 mutation.

Villanueva-Mendoza, Cristina

Familial case of Blau syndrome associated with a CARD15/NOD2 mutation. [electronic resource] - Ophthalmic genetics Sep 2010 - 155-8 p. digital

Publication Type: Case Reports; Journal Article

1744-5094

10.3109/13816810.2010.492818 doi


Adult
Arthritis, Rheumatoid--genetics
Exanthema--genetics
Female
Fluorescein Angiography
Humans
Joint Diseases--genetics
Nod2 Signaling Adaptor Protein--genetics
Pedigree
Point Mutation
Polymerase Chain Reaction
Recurrence
Syndrome
Uveitis, Anterior--genetics
Young Adult