%0 Journal Article
%T Holt Oram Syndrome associated with congenital panhypopituitarism rare
association: A case report
%A Abdulmoein E Al-Agha
%A Lujain K AlFarran
%A Melissa G Al Beiruty
%J -
%D 2018
%X Holt Oram Syndrome (HOS) is a genetic condition characterized by varies skeletal and cardiac anomalies. However, HOS associated with panhypopiuitarism has never been reported. Thus, we reported a case of a 25 days old male neonate with bilateral absent radius, short curved ulnar, absent thumbs and micropenis associated with recurrent episode of persistent hypoglycemia, due to hypopituitarism
%K Neonate
%K Holt Oram
%K Skeletal abnormality
%K Hypoglycemia
%K Hypopituitarism
%U https://www.alliedacademies.org/articles/holt-oram-syndrome-associated-with-congenital-panhypopituitarism-rareassociation-a-case-report-10402.html