2018
DOI: 10.5125/jkaoms.2018.44.4.198
|View full text |Cite
|
Sign up to set email alerts
|

Classical oral manifestations of Dyke-Davidoff-Masson syndrome: a case report with review of the literature

Abstract: Dyke-Davidoff-Masson syndrome is a non-inherited rare condition that presents during childhood and is characterized by seizures, hemiplegia, mental retardation, cerebral hemiatrophy, calvarial thickening, and hyperpneumatization of the frontal sinuses. The present article highlights a case of a 12-year-old male child with additional clinical findings of café-au-late pigmentation and ocular lipodermoid. This is the first case report of Dyke-Davidoff-Masson syndrome to describe oral manifestations, such as unila… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

0
5
0

Year Published

2021
2021
2023
2023

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 9 publications
(5 citation statements)
references
References 21 publications
(32 reference statements)
0
5
0
Order By: Relevance
“…While the symptoms of the infantile variety first appear during pregnancy or infancy, those of the acquired kind first show up throughout puberty or adulthood [8]. In a few cases, there may be ipsilateral Café au lait pigmentations and ocular lipodermoid, contralateral delayed teeth eruption, hypoplasia, and taurodontism [9]. The signs of DDMS may be so minor that conventional radiographs fail to pick them up.…”
Section: Discussionmentioning
confidence: 99%
“…While the symptoms of the infantile variety first appear during pregnancy or infancy, those of the acquired kind first show up throughout puberty or adulthood [8]. In a few cases, there may be ipsilateral Café au lait pigmentations and ocular lipodermoid, contralateral delayed teeth eruption, hypoplasia, and taurodontism [9]. The signs of DDMS may be so minor that conventional radiographs fail to pick them up.…”
Section: Discussionmentioning
confidence: 99%
“…The congenital form states that the cerebral insult likely occurred in-utero due to vascular malformation, cerebral infarction, coarctation of the mid-aortic arch, gestational vascular occlusion, and infections. In the acquired form, the cerebral insult likely occurred during the perinatal or postnatal period, caused by hypoxia, birth trauma, tumors, infections, prolonged febrile seizures, and intracranial hemorrhage [8]. In both sexes, either of the hemispheres can be affected by DDMS.…”
Section: Discussionmentioning
confidence: 99%
“…In contrast, we report adult population in northern Tanzania to have brain atrophy which is not associated with paranasal infection. Although, the enlargement of the paranasal sinuses, mastoid cells and calvarial thickening have been reported in patients with cerebral hemi-atrophy [ 48 , 49 ]. As the pathogenesis of sinusitis to the central nervous system (CNS) has not been well explored globally.…”
Section: Discussionmentioning
confidence: 99%