SELECT ISSUE

Romanian Journal of Neurology, Volume XV, No. 4, 2016
ISSN 1843-8148  |  e-ISSN 2069-6094
ISSN-L 1843-8148
DOI: 10.37897/RJN

Indexed

DOI - Crossref
Similarity Check by iThenticate, worldwide No 1 professional plagiarism checking system
DOAJ
Scopus
Ebsco Host - Medline
Google Academic
Semantic Scholar

HIGHLIGHTS

ICMJE- Recommendations

Read the Recommendations for the Conduct, Reporting, Editing, and Publication of Scholarly work in Medical Journals.

Promoting Global Health

The published medical research literature is a global public good. Medical journal editors have a social responsibility to promote global health by publishing, whenever possible, research that furthers health worldwide.

THREE CASE SERIES INVOLVING PROGRESIVE MOTOR DEFICIT

, , and

ABSTRACT

The muscular dystrophyes are a group of inherited, non-inflamatory disorders, consisting of progresive muscle wasting, without perripheral or central nerve involvement. We present a series of three cases involving progresive motor deficit and their different evolutions. The first case is about a 57 year old female patient, without a significant family medical history, presenting for progresive motor deficit involving the shoulder and pelvic muscles, started at the age of 20 year old, when she was diagnosed with a sporadic form of limb-girdle muscular dystrophy. The second case is about a 27 year old male, diagnosed with muscular dystrophy at the age of 15. The third case is about a 43 year old male admitted for frequent falls and weakness of the limbs, mainly distal, started 10 years ago. He was diagnosed with myotonic dystrophy. Although there is still no treatment for muscular dystrophies, the pathology is under investigation in clinical trials.

Keywords: fetal stroke, alloimmune/autoimune thrombocytopenia, intracranial hemorrhage, neurological consequences

Full text | PDF