Mucopolysaccharidosis type 2

A lysosomal storage disease with multisystemic involvement leading to a massive accumulation of glycosaminoglycans and a wide variety of symptoms including distinctive coarse facial features, short stature, cardio-respiratory involvement and skeletal abnormalities. It manifests as a continuum varying from a severe form with neurodegeneration to an attenuated form without neuronal involvement.

Atrioventricular block

Delayed or lack of conduction of atrial depolarizations through the atrioventricular node to the ventricles.

Total: 3

(per page)

PMID (PMCID)
29506582	MALE
	Early childhood onset of high-grade atrioventricular block in Hunter syndrome.
	Chlebowski MM, Heese BA, Malloy-Walton LE. Cardiol Young. 2018;28(5):786-787.
	We present a case of a 3-year-old boy with Hunter syndrome who was found to have various degrees of atrioventricular block.
29506582	MALE
	Early childhood onset of high-grade atrioventricular block in Hunter syndrome.
	Chlebowski MM, Heese BA, Malloy-Walton LE. Cardiol Young. 2018;28(5):786-787.
	Early childhood onset of high-grade atrioventricular block in Hunter syndrome.
29506582	MALE
	Early childhood onset of high-grade atrioventricular block in Hunter syndrome.
	Chlebowski MM, Heese BA, Malloy-Walton LE. Cardiol Young. 2018;28(5):786-787.
	To date, there have been no reports of early childhood onset of high-grade atrioventricular block in patients with Hunter syndrome.