2021
DOI: 10.1212/wnl.0000000000012488
|View full text |Cite
|
Sign up to set email alerts
|

Clinical Reasoning: A 59-Year-Old Man With Progressive Proximal Weakness Since Childhood

Abstract: His gait was slow with a decreased stride length and narrow base. Sensory exam was normal. Questions for consideration:1. Where would you localize this process? 2. Is this an acquired or inherited disease?3. What testing would be helpful to narrow the differential? Section 2Given the lack of sensory involvement, possible localizations include anterior horn cells, motor nerve roots, neuromuscular junction, and muscles. His presentation of symmetrical biceps and lower

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
0
0

Year Published

2023
2023
2023
2023

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
(1 citation statement)
references
References 12 publications
0
0
0
Order By: Relevance
“…Another differential with similar pathologic findings is X-linked recessive myopathy with excessive autophagy (XMEA). However, XMEA, which also has proximal muscle weakness, lacks other systemic features of DD [ 6 ].…”
Section: Discussionmentioning
confidence: 99%
“…Another differential with similar pathologic findings is X-linked recessive myopathy with excessive autophagy (XMEA). However, XMEA, which also has proximal muscle weakness, lacks other systemic features of DD [ 6 ].…”
Section: Discussionmentioning
confidence: 99%