Sign Up to like & get
recommendations!
1
Published in 2018 at "World Journal of Clinical Cases"
DOI: 10.12998/wjcc.v6.i14.800
Abstract: Carney complex (CNC) is an extremely rare genetic syndrome of pigmented skin lesions, endocrine hyperfunction and myxoma. Given its diverse clinical manifestations, CNC is often misdiagnosed. Recognition of some special clinical manifestations and imaging features…
read more here.
Keywords:
carney complex;
review literature;
complex two;
case reports ... See more keywords
Sign Up to like & get
recommendations!
1
Published in 2022 at "International journal of clinical pharmacology and therapeutics"
DOI: 10.5414/cp204190
Abstract: Hereditary transthyretin amyloidosis (hATTR) is an ultra-rare illness. Inotersen is a 2'-O-methoxyethyl (2'MOE)-modified antisense oligonucleotides (ASO) approved in 2018 as a polyneuropathy treatment for adults with hereditary transthyretin amyloidosis stages 1 or 2. Inotersen can…
read more here.
Keywords:
case reports;
severe thrombocytopenia;
thrombocytopenia;
reports review ... See more keywords