Rare Disease Report

LAL Deficiency: One Man's Long Journey to Diagnosis and Treatment

JULY 03, 2015

Brett Billmeyer of the LAL Solace Patient Community tells of his arduous journey that led to his diagnosis - and eventual management - of lysosomal acid lipase (LAL) deficiency.

For more information, visit http://www.lalsolace.org/

Stay informed on the latest rare disease news and developments by signing up for our newsletter.
Copyright © RareDR 2013-2018 Rare Disease Communications. All Rights Reserved.