𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Smothering dystonia in a patient with oromandibular dystonia

✍ Scribed by Stephen Grill


Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
46 KB
Volume
19
Category
Article
ISSN
0885-3185

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

A case report is presented of a patient with pathologically confirmed striatonigral degeneration who experienced episodic syncope as a result of oromandibular dystonia obstructing inhalation through her mouth and nose. Β© 2004 Movement Disorder Society


πŸ“œ SIMILAR VOLUMES


Secondary nonresponsiveness to botulinum
✍ Charles H. Adler; Stewart A. Factor; Mitchell Brin; Kapil D. Sethi πŸ“‚ Article πŸ“… 2001 πŸ› John Wiley and Sons 🌐 English βš– 77 KB

## Abstract Intramuscular injection of botulinum toxin type A is the treatment of choice for most cases of oromandibular dystonia. We report on five patients with oromandibular dystonia that developed secondary nonresponsiveness to botulinum toxin type A following multiple injections over a 6‐year

Dystonia in a patient with ring chromoso
✍ Craig E. Hou; Bradley L. Schlaggar; Brad A. Racette πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 English βš– 51 KB

## Abstract Dystonia associated with chromosomal abnormalities is typically attributed to chromosomal deletions. We describe a patient with ring chromosome 21, with karyotype 46XX,r(21)(p11.2q22.3); 46,XX,dic r(21)(p11.2q22.3); 45, XX, –21, who developed childhood onset cervical dystonia. Β© 2003 Mo

Dystonia in a patient with deletion of 1
✍ Dr. Mark Forrest Gordon; Susan Bressman; Mitchell F. Brin; Deborah de Leon; Doro πŸ“‚ Article πŸ“… 1995 πŸ› John Wiley and Sons 🌐 English βš– 347 KB

## Abstract This is the first reported case of dystonia with a partial deletion of the long arm (q) of chromosome 18. Neurologic findings in the 18q‐ syndrome include mental retardation, seizures, nystagmus, incoordination, tremor, and chorea. A 36‐year‐old woman with an 18q terminal deletion [Kary

Adductor laryngeal breathing dystonia in
✍ Dr. M. F. Lew; M. Shindo; C. B. Moskowitz; K. C. Wilhelmsen; S. Fahn; C. H. Wate πŸ“‚ Article πŸ“… 1994 πŸ› John Wiley and Sons 🌐 English βš– 308 KB

## Abstract We report a patient with Lubag (X‐linked dystonia‐parkinsonism) who presented with severe respiratory stridor form adductor laryngeal breathing dystonia. Emergency tracheostomy was necessary, and subsequent laryngeal injection with botulinum toxin led to worsening aspiration. Botulinum