Format

Send to

Choose Destination
J Stroke Cerebrovasc Dis. 2019 Sep 4:104354. doi: 10.1016/j.jstrokecerebrovasdis.2019.104354. [Epub ahead of print]

A Case of Leukoencephalopathy and Small Vessels Disease Caused by a Novel HTRA1 Homozygous Mutation.

Author information

1
Department of Neurology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.
2
Department of Medical Genetics, Umraniye Training and Research Hospital, Health Sciences University, Istanbul, Turkey.
3
Department of Neurology, Sultan Abdulhamid Han Training and Research Hospital, Health Sciences University, Istanbul Turkey.
4
Council of Forensic Medicine, Istanbul, Turkey. Electronic address: nhakcakaya@gmail.com.

Abstract

Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL) is a heritable, rare small vessel disease, which is caused by HTRA1 mutations and mostly reported Japanese and Chinese population. CARASIL is an orphan disease, which presents with progressive motor and cognitive impairment, alopecia, and spondylosis. The disease typically starts with lumbago at early twenties. Ischemic strokes start at mid-twenties. Patients have no cardiovascular or any other risk factors. Multiple lacunar infarcts and leukoencephalopathy cause progressive neurologic involvement. Leukoencephalopathy and small vessel disease without any risk factors is a significant finding for the differential diagnosis of HTRA1 gene pathology. This report presents clinical and genetic features of a rare case of typical CARASIL from Turkey who was followed with uncertain diagnoses for years.

KEYWORDS:

CARASIL; HTRA1; lacunar infarcts; leukoencephalopathy; small vessel disease

Supplemental Content

Full text links

Icon for Elsevier Science
Loading ...
Support Center