ArticleCureus2025
Pontine Tegmental Cap Dysplasia: A Rare Case in South Africa.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
We present the first case of pontine tegmental cap dysplasia (PTCD) reported in South Africa, involving a one-year-old girl with bilateral sensorineural deafness, global atrophy, hemivertebrae, and butterfly vertebrae. Clinical examination revealed subtle dysmorphic features, abnormal corneal sensation, bilateral strabismus, and uncertain visual acuity. Magnetic resonance imaging (MRI) demonstrated key diagnostic features, including ventral pons hypoplasia, ectopic dorsal pontine tissue, and cranial nerve abnormalities such as hypoplasia of the facial nerves, absent right vestibulocochlear nerve, and non-branching left vestibulocochlear nerve. A review of the literature highlights the importance of advanced neuroimaging techniques, such as MRI and diffusion tensor imaging (DTI), in identifying the structural aberrations and potential axonal guidance abnormalities associated with PTCD. This case report aims to shed light on this rare condition's intricacies and emphasize the need for further research to deepen our understanding and enhance patient care outcomes.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.