The trismus-pseudocampylodactyly syndrome.
نویسندگان
چکیده
منابع مشابه
Trismus Pseudocamptodactyly Syndrome: A Sporadic Cause of Trismus
Trismus pseudocamptodactyly syndrome is a very rare autosomal dominant inherited disorder characterized by the inability to completely open the mouth (trismus) and the presence of abnormally short tendon units causing the fingers to curve (camptodactyly). Early diagnosis and management of this condition is important to prevent facial deformities in the patient. Reporting such a case is importan...
متن کاملTrismus-pseudocamptodactyly syndrome: case report ten years after.
BACKGROUND In 1969, Hecht and Beals described for the first time a rare dominant autosomal syndrome characterised by reduced mouth opening, pseudocamptodactyly, short stature, and foot deformities. Recent studies have confirmed that TPS is caused by a mutation of MYH8 that is common to another disease called Carney syndrome. CASE REPORT The authors describe the long term follow-up of a case p...
متن کاملDevelopment of dysphagia and trismus developed after c1-2 posterior fusion in extended position.
Cervical misalignment after upper cervical fusion including the occipital bone may cause trismus or dysphagia, because the occipito-atlanto joint is associated with most of the flex and extended motion of the cervical spine. There are no reports of dysphagia and trismus after C1-2 fusion. The purpose of this paper is to demonstrate the potential risk of dysphagia and trismus even after upper ce...
متن کاملHorner's syndrome in severe tetanus.
A 66 year old man was admitted with a left Horner's syndrome, and trismus due to tetanus. Three days later he had respiratory arrests, classical tetanic spasms and was ventilated. He had associated severe autonomic dysfunction, tachyarrhythmias, hypotension, sweating and constipation. There was complete resolution of the left Horner's syndrome with recovery from tetanus.
متن کاملMouth opening limitation caused by coronoid hyperplasia: a report of four cases
Coronoid process hyperplasia is a rare condition that causes mouth opening limitation, otherwise known as trismus. The elongated coronoid processes impinge on the medial surfaces of the zygomatic arches when opening the mouth, which limits movement of the mandible and leads to trismus. Patients with trismus due to coronoid process hyperplasia do not have any definite symptoms such as temporoman...
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ورودعنوان ژورنال:
- Journal of medical genetics
دوره 11 1 شماره
صفحات -
تاریخ انتشار 1974