Orbicularis oculi myectomy as a treatment for blepharospasm in a case of Schwartz Jampel syndrome

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Orbicularis Oculi Myectomy as a Treatment for Blepharospasm in a Case of Schwartz Jampel Syndrome

PURPOSE To describe a patient with Schwartz Jampel vel Aberfeld syndrome (SJS) who underwent orbicularis oculi myectomy as a treatment for blepharospasm. CASE REPORT A 4-year-old child with SJS did not respond to an injection of a single dose of botulinum toxin after one month, so orbicularis myectomy was then performed under general anesthesia. During the procedure, orbicularis vermiform mov...

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Schwartz-Jampel syndrome. A case report.

A rare case of Schwartz-Jampel Syndrome is reported. Its main oral and facial manifestations are highlighted.

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Schwartz-Jampel syndrome.

This is a report of a very rare case of Schwartz Jampel syndrome, with few unusual findings, in a 13 years girl from Nepal, who concurrently also had superotemporal subluxation of the crystalline lens along with blepharophimosis syndrome.

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The Schwartz-Jampel Syndrome. A Minireview

The Schwartz-Jampel Syndrome (SJS) is a very rare condition characterised by Constant fìndings such as typical facial appearance, muscle hypertrophy and continuous muscle activity. Other fìndings are more or less frequently associated, especially skeletai abnormalities, including dwarfism or anyway short stature. The Authors review thè literature about this condition analysing thè clinical pict...

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Schwartz-Jampel syndrome (chondrodystrophic myotonia).

Schwartz-Jampel syndrome is a rare autosomal recessive disorder. Joint contractures, generalised myotonia, skeletal anomalies, and facial dysmorphism are common features; malignant hyperthermia is a potentially lethal complication during anaesthesia.

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ژورنال

عنوان ژورنال: Journal of Ophthalmic and Vision Research

سال: 2016

ISSN: 2008-322X

DOI: 10.4103/2008-322x.188401