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Article

Rapidly progressive multiple system atrophy in a patient carrying LRRK2 G2019S mutation.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology - 1 Jan 2024

Carrer Tommaso, Bonato Giulia, Sandre Michele, Emmi Aron, Campagnolo Marta, Musso Giulia, Carecchio Miryam, Parchi Piero, Antonini Angelo

Abstract excerpt

BACKGROUND: Multiple system atrophy (MSA) is considered a primarily sporadic neurodegenerative disease, but the role of genetic is poorly understood. CASE: We present a female patient of Moroccan origin who developed a rapidly progressive non-levodopa responsive parkinsonism, gait and balance problems, and dysautonomia including severe bulbar symptoms. She was diagnosed with MSA Parkinsonian-type (MSA-P) and...

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Identifiers

PMID: 37752324
DOI: 10.1007/s10072-023-07056-5

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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