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Late infantile neuronal ceroid lipofuscinosis

Late infantile neuronal ceroid lipofuscinoses (LINCLs) are a genetically heterogeneous group of neuronal ceroid lipofuscinoses (NCLs; see this term) typically characterized by onset during infancy or early childhood with decline of mental and motor capacities, epilepsy, and vision loss through retinal degeneration.

Bradycardia

A slower than normal heart rate (in adults, slower than 60 beats per minute).

Total: 1

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PMID (PMCID)
22221116	MIXED_SAMPLE	Child
	Progressive conduction defects and cardiac death in late infantile neuronal ceroid lipofuscinosis.
	Fukumura S, Saito Y, Saito T, Komaki H, Nakagawa E, Sugai K, Sasaki M, Oka A, Takamisawa I. Dev Med Child Neurol. 2012;54(7):663-6.
	This article reports the case of a female with late infantile neuronal ceroid lipofuscinosis who developed right and left anterior bundle branch blocks and episodic bradycardia at 23 years of age.