WAGR syndrome : autosomal dominant,
C/f: willms tumour with aniridia
Genetics: region on short arm of chr 11.
PAX6, WT1 genes
C/f: willms tumour with aniridia
Genetics: region on short arm of chr 11.
PAX6, WT1 genes
Cone rod dystrophy::
30 genes identified out of them 20 are AR.
ABC4 is most commonly involved.
30 genes identified out of them 20 are AR.
ABC4 is most commonly involved.
No comments:
Post a Comment