Skip to Content

panhypopituitary dwarfism


Definition: type I is an autosomal recessive disorder with a deficient human growth hormone (ACTH, FSH that delays sexual development, and produces hypothyroidism and adrenal insufficiency; type II is similar but is an X-linked disorder.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

© Copyright 2018 Wolters Kluwer. All Rights Reserved. Review date: Sep 19, 2016.