ケーザー症候群
WordNet
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
PrepTutorEJDIC
- (疾患の徴候となる一群の)症徴候,症候群 / (事件・社会的状態などのパターンを示す)徴候形態
English Journal
- Fourth cranial nerve palsy and Brown syndrome: two interrelated congenital cranial dysinnervation disorders?
- Kaeser PF1, Brodsky MC.
- Current neurology and neuroscience reports.Curr Neurol Neurosci Rep.2013 Jun;13(6):352. doi: 10.1007/s11910-013-0352-5.
- Based on neuroimaging data showing absence of the trochlear nerve, congenital superior oblique palsy is now classified as a congenital cranial dysinnervation disorder. A similar absence of the abducens nerve is accompanied by misinnervation to the lateral rectus muscle from a branch of oculomotor ne
- PMID 23636931
- A survey of paediatric HIV programmatic and clinical management practices in Asia and sub-Saharan Africa--the International epidemiologic Databases to Evaluate AIDS (IeDEA).
- IeDEA Pediatric Working Group.
- Journal of the International AIDS Society.J Int AIDS Soc.2013 Jan 15;16(1):17998. doi: 10.7448/IAS.16.1.17998.
- INTRODUCTION: There are limited data on paediatric HIV care and treatment programmes in low-resource settings.METHODS: A standardized survey was completed by International epidemiologic Databases to Evaluate AIDS paediatric cohort sites in the regions of Asia-Pacific (AP), Central Africa (CA), East
- PMID 23336728
- Absence of the fourth cranial nerve in congenital Brown syndrome.
- Kaeser PF1, Kress B, Rohde S, Kolling G.
- Acta ophthalmologica.Acta Ophthalmol.2012 Jun;90(4):e310-3. doi: 10.1111/j.1755-3768.2011.02354.x. Epub 2012 Jan 23.
- PURPOSE: To elucidate the aetiology of congenital Brown syndrome.METHODS: Four consecutive patients diagnosed with unilateral congenital Brown syndrome had a comprehensive standardized ocular motility examination. Any compensatory head posture was measured. Brain magnetic resonance imaging (MRI) wit
- PMID 22268674
Related Links
- #181400 Scapuloperoneal syndrome, neurogenic, Kaeser type (SCPNK) (Kaeser syndrome) (Stark-Kaeser syndrome) (Scapuloperoneal syndrome, neurogenic type, of Kaeser) 肩甲腓骨筋症候群, 神経原性, Kaeser 型) (Kaeser 症候群)
- Kaeser syndrome symptoms, causes, diagnosis, and treatment information for Kaeser syndrome (Scapuloperoneal myopathy) with alternative diagnoses, full-text book chapters, misdiagnosis, research treatments, prevention, and ...
- Clinical Synopsis TEXT A number sign (#) is used with this entry because this form of neurogenic scapuloperoneal syndrome (SCPNK) is caused by mutation in the gene encoding desmin (DES; 125660) on chromosome 2q35.
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