Two patients are described who developed action, reflex myoclonus during acute renal failure. In both cases the myoclonus was abolished after the intravenous administration of clonazepam. We suggest that the characteristic action myoclonus, which occurs in both acute renal failure and postanoxic encephalopathy, is caused by a disturbance of function in the lower brainstem reticular formation.

18 neonates aged 5-60 days with Benign neonatal sleep myoclonus were identified. Fifteen neonates had been misdiagnosed as neonatal seizures before referral. All treatments were withdrawn once the diagnosis of benign neonatal sleep myoclonus was made. Benign neonatal sleep myoclonus should be considered early in the differential diagnosis of neonatal seizures.

background : this study evaluated the sensation of palatal ucosa before and after le fort i osteotomy and compared it based on whether greater palatine nerve has been dissected or not. methods : sixteen patients were studied within one week before  urgery and then one week, 6 weeks, 3 months and 6 months after surgery. four tests including sharp-blunt discrimination, cold perception, pin prick ...

Background: To evaluate the role of different morphological palatal rugae patterns (palatal print) as a tool for personal identification. Method: A pilot cross-sectional study was carried out on 60 Egyptian subjects and 60 Malaysian subjects. All were above 6 years old, nonsmokers and were sharing the same dietary habits. Palatal impressions were taken from the subjects and a rugogram was issue...

BACKGROUND North Sea Progressive Myoclonus Epilepsy is a rare and severe disorder caused by mutations in the GOSR2 gene. It is clinically characterized by progressive myoclonus, seizures, early-onset ataxia and areflexia. As in other progressive myoclonus epilepsies, the efficacy of antiepileptic drugs is disappointingly limited in North Sea Progressive Myoclonus Epilepsy. The ketogenic diet an...

A patient with post-hypoxic myoclonus, sensitive to therapy with 5-hydroxytryptophan and clonazepam, was subjected to detailed electrophysiological investigation. Brief generalised jerks followed the critical stimulus of muscle stretch. The electroencephalogram showed generalised spikes that were associated with, but not time locked to, the myoclonus. The cranial nerve nuclei were activated up...

Nonsyndromic familial hyperdontia/supernumerary teeth is a rare disorder of odontogenesis characterized by an excess number of teeth with familial background. They can be supplemental (resembling natural teeth), conical, tuberculate or molariform. Early clinical and radiographic examination of the supernumerary teeth allow for optimal yet minimal treatment. This article reports two rare cases o...

Clear cell myoepithelioma arising from the minor salivary glands of hard palate is a rare entity. Most of the cases of palatal myoepitheliomas reported so far are either plasmacytoid or spindle cell type. Our literature search revealed only one case report of clear cell myoepithelioma of the palate. We report a case in a 21-year-old female who presented to us with a non-ulcerating, painless fir...

Introdouction: Variations in root canal morphology pose a challenge for successful endodontic treatment. The root canal anatomy of the maxillary first molar has been often described as three roots with four canals (two mesiobuccal, one distobuccal, and one palatal). The occurrence of two palatal canals in one palatal root is quite rare. This report represents the case of a maxillary first molar...

Piracetam, a derivative of gamma-aminobutyric acid (GABA), has been used extensively for treatment of myoclonus in a variety of conditions, but not in patients with idiopathic generalized epilepsy (IGE). We have treated a patient with juvenile myoclonic epilepsy who had frequent and inconvenient morning myoclonus with 3,200 mg of piracetam daily. She had had only two generalized tonic-clonic se...