https://www.selleckchem.com/products/jdq443.html
Pituitary blastoma is a rare, dysontogenetic hypophyseal tumor of infancy first described in 2008, strongly suggestive of DICER1 syndrome. This work aims to describe genetic alterations, clinical courses, outcomes, and complications in all known pituitary blastoma cases. A multi-institutional case series is presented from tertiary pediatric oncology centers. Patients included children with pituitary blastoma. Genetic testing, surgery, oncologic therapy, endocrine support are reported. Outcome measures included survival, long-term morbidi
Beğen
Yorum Yap
Paylaş
