Hyperekplexia in a girl with posterior fossa malformations

Journal of Child Neurology

Volumn 17, Issue 2, 2002, Pages 147-149

  Goraya, Jatinder S ^a   Shah, Durlabh ^a   Poddar, Banani ^a  

^a GOVERNMENT MEDICAL COLLEGE AND HOSPITAL   (India)

Author keywords

[No Author keywords available]

Indexed keywords

CARBAMAZEPINE; CLONAZEPAM; PHENOBARBITAL; PHENYTOIN;

ARTICLE; BRAIN STEM INJURY; CASE REPORT; CIRCADIAN RHYTHM; CLINICAL FEATURE; DISEASE ASSOCIATION; DRUG RESPONSE; FEMALE; HUMAN; NEUROPATHOLOGY; POSTERIOR FOSSA; PRIORITY JOURNAL; SCHOOL CHILD; SKULL MALFORMATION; SOUND; STARTLE EPILEPSY; STARTLE REFLEX; STIMULUS RESPONSE; SYMPTOMATOLOGY; TOUCH;

EID: 0036257442     PISSN: 08830738     EISSN: None     Source Type: Journal    
DOI: 10.1177/088307380201700213     Document Type: Article

References (11)

1. Startle disease or hyperekplexia: Further delineation of the syndrome
2. Audiogenic startle reflex of man and its relationship to startle syndrome. A review
3. The hyperekplexias and their relationship to the normal startle reflex
4. 1 subunit of the inhibitory glycine gene receptor cause the dominant neurological disorder, hyperekplexia
5. A patient with reflex myoclonus and muscle rigidity: "Jerking stiff-man syndrome"
6. Hyperekplexia and trismus due to brainstem encephalopathy
7. Hyperekplexia in a patient with a brainstem vascular anomaly
8. Hyperekplexia: Abnormal startle response due to glycine receptor mutations
9. Mutational analysis of familial and sporadic hyperekplexia
10. Congenital malformations of the brain
11. Early fatal pontocerebellar hypoplasia in premature twin sisters