1970
DOI: 10.1001/archotol.1970.00770040782012
|View full text |Cite
|
Sign up to set email alerts
|

Temporal Bone Findings in Trisomy 18 Syndrome

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

0
4
0

Year Published

1975
1975
2021
2021

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 35 publications
(4 citation statements)
references
References 9 publications
0
4
0
Order By: Relevance
“…Although anomalies of the auditory organ have been noticed in more than 50 per cent of cases, only a few reports have described in detail the histopathological changes in the temporal bone. [2][3][4][5][6][7][8][9] In this FP = footplate of stapes; F = facial nerve; CT = chorda tympani. report, the histopathological ndings of anomalies in the temporal bone of this syndrome are described.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Although anomalies of the auditory organ have been noticed in more than 50 per cent of cases, only a few reports have described in detail the histopathological changes in the temporal bone. [2][3][4][5][6][7][8][9] In this FP = footplate of stapes; F = facial nerve; CT = chorda tympani. report, the histopathological ndings of anomalies in the temporal bone of this syndrome are described.…”
Section: Discussionmentioning
confidence: 99%
“…To date, the histopathological ndings of the temporal bone have been reported in only a few patients with the trisomy 18 syndrome. [2][3][4][5][6][7][8][9] Here we report the temporal bone histopathological ndings in a stillborn fetus with trisomy 18 syndrome, including a three-dimensional reconstruction of the anomalous auditory ossicles.…”
Section: Introductionmentioning
confidence: 94%
“…In CHARGE syndrome it is typical to detect abnormalities in all the semicircular canals [71]. On the other hand, a partial involvement can be observed in trisomy 13, in which lateral semicircular canal defects are most common and are present with or without superior or posterior semicircular canal abnormalities, while in trisomy 18, the defects frequently affect the lateral and superior semicircular canals [72]. Isolated agenesis of the posterior semicircular canals, without involvement of the lateral semicircular canals, is extremely rare but has been detected in Waardenburg syndrome type II patients [73].…”
Section: Posterior Labyrinth Anomaliesmentioning
confidence: 99%
“…Studying the temporal bones of patients with chromosomal disorders provides an opportunity to identify the association of certain ear anomalies with specific chromosomal abnormalities. Ear anomalies affecting the external, middle, and inner ear have been documented in temporal bone studies of patients with chromosomal disorders such as trisomy 13 (Patau Syndrome) [2][3][4][5], trisomy 18 (Edwards Syndrome) [6,7], trisomy 21 (Down Syndrome) [8][9][10][11], trisomy 22 [12], 4pÀ (Wolf-Hirschhorn Syndrome) [13][14][15], and Turner Syndrome [16,17]. The nature and extent of ear anomalies vary according to the particular chromosomal aberration that may be present.…”
Section: Introductionmentioning
confidence: 99%