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

Congenital cataract, facial dysmorphism and demyelinating neuropathy (CCFDN) in 10 Czech Gypsy children--frequent and underestimated cause of disability among Czech Gypsies.

Lassuthova P1, Sišková D, Haberlová J, Sakmaryová I, Filouš A, Seeman P.
Orphanet journal of rare diseases.Orphanet J Rare Dis.2014 Apr 1;9:46. doi: 10.1186/1750-1172-9-46.
BACKGROUND: Congenital Cataract Facial Dysmorphism and demyelinating Neuropathy (CCFDN, OMIM 604468) is an autosomal recessive multi-system disorder which was first described in Bulgarian Gypsies in 1999. It is caused by the homozygous founder mutation c.863 + 389C > T in the CTDP1 gene. The synd
PMID 24690360

Telencephalosynapsis (synencephaly) and rhombencephalosynapsis with posterior fossa ventriculocele ('Dandy-Walker cyst'): an unusual aberrant syngenetic complex.

Sergi C1, Hentze S, Sohn C, Voigtländer T, Jung C, Schmitt HP.
Brain & development.Brain Dev.1997 Sep;19(6):426-32.
Agenesis of the cerebellar vermis (paleocerebellar agenesis) with fusion of the cerebellar hemispheres (rhombencephalosynapsis) is a rare malformation of the central nervous system (CNS). Its combination with synencephaly (telencephalosynapsis), telencephalic ventricular aplasia, aqueductal atresia
PMID 9339873

Magnetic resonance imaging in the diagnosis of dominantly inherited cerebello-olivary atrophy: a clinicopathologic study.

Bonni A1, del Carpio-O'Donovan R, Robitaille Y, Andermann E, Andermann F, Arnold DA.
Canadian Association of Radiologists journal = Journal l'Association canadienne des radiologistes.Can Assoc Radiol J.1993 Jun;44(3):194-8.
To facilitate the study of cerebellar degenerative disorders, improved clinical diagnosis is needed. Cerebello-olivary atrophy is pathologically distinct, but until now its diagnosis has been thought to require postmortem examination. This condition was considered as a possible diagnosis in two pati
PMID 8504332

Related Links

⚡Presentation "Cerebellar dysfunction, syndromes, signs ...

Lesion location 1 vermis (damage to midline structures) - paleocerebellar syndrome - disturbance of equilibrium hemisphere structures of the cerebellum - neocerebellar syndrome - impaired limb co- ordination cerebellar connections to ...

[Standing ataxia in cerebellar lesions. Differential diagnosis ...

ABSTRACT Several forms of postural ataxia can be distinguished in cerebellar lesions by quantitative analysis of stance, a paleocerebellar, a vestibulocerebellar and a neocerebellar syndrome, for each of which a different underlying ...