Limb-girdle myasthenia, nonfamilial (Q92774): Difference between revisions

← Older edit

@@ Property / CURIE @@
+CID11:ID_697826513
@@ Property / CURIE: CID11:ID_697826513 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_697826513
@@ Property / Canary Token: dki-india-ID_697826513 / rank @@
+Normal rank
@@ Property / Verification Status @@
+Concluído
@@ Property / Verification Status: Concluído / rank @@
+Normal rank
@@ Property / Knowledge Architect @@
+https://pauloleads.com.br/cases-publicos/
+Normal rank
@@ Property / Collection date @@
+August 2026Timestamp +2026-08-15T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-15T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 15 August 2026 / rank @@
+Normal rank

Latest revision as of 07:54, 16 August 2026

Limb-girdle myasthenias are rare conditions in which impaired neuromuscular transmission leads to weakness of proximal limb muscles with little or no involvement of the ocular, bulbar or facial muscles, giving rise to a characteristic “waddling” gait. In most of these patients the onset of muscle weakness is first noticed in infancy or childhood, but a later onset is described. Nonfamilial limb-girdle myasthenia include autoimmune forms.

Language	Label	Description	Also known as
default for all languages	ID_697826513
English	Limb-girdle myasthenia, nonfamilial	Limb-girdle myasthenias are rare conditions in which impaired neuromuscular transmission leads to weakness of proximal limb muscles with little or no involvement of the ocular, bulbar or facial muscles, giving rise to a characteristic “waddling” gait. In most of these patients the onset of muscle weakness is first noticed in infancy or childhood, but a later onset is described. Nonfamilial limb-girdle myasthenia include autoimmune forms.