Presentation
The features of Sakoda complex present in these patients may also overlap with frontonasal dysplasia and morning glory syndrome suggesting shared pathogenic relationships. [pubmed.ncbi.nlm.nih.gov]
The approach we present in this article might be used in a variety of social research fields. [nature.com]
Entire Body System
- Epilepsy
Abnormalities of gyration, heterotopias, tuberous sclerosis, focal cortical dysplasia, microdysgenesis, dysembryoplastic neuroepithelial tumour and dysgenesis of the archicortex in epilepsy. [pubmed.ncbi.nlm.nih.gov]
It has been reported in association with ophthalmologic abnormalities, cognitive deficits and severe epilepsy. [inis.iaea.org]
Associated abnormalities include optic disc dysplasia, microphthalmia, cortical dysgenesis, mental retardation and epilepsy. The etiology remains unknown. [humpath.com]
- Atrial Septal Defect
Synopsis sphenoethmoidal encephalomeningocele cleft palate microphthalmia optic nerve hypoplasia diffuse pachygyria asymmetric ventricles atrial septal defect hemivertebrae renal abnormalities absence of the right hemisphere bifid thumb Differential diagnosis [humpath.com]
The first patient also has right microphthalmia, optic nerve hypoplasia, diffuse pachygyria, asymmetric ventricles, atrial septal defect, hemivertebrae, and renal abnormalities. [pubmed.ncbi.nlm.nih.gov]
Face, Head & Neck
- Median Cleft Lip
[Sphenoethmoidal meningoencephalocele associated with agenesis of corpus callosum and median cleft lip and palate--report of two cases (author's transl)]. Sakoda K, Uozumi T, Hirakawa K, Harada Y, Chikuie S, Sasaki U, Ibuki Y. Sakoda K, et al. [pubmed.ncbi.nlm.nih.gov]
cleft lip and palate. [link.springer.com]
cleft lip and palate: case report. [syndromefinder.ncchd.go.jp]
Treatment
Unless there is early detection with curative treatment, the 5-year survival rate of advanced HCC is less than 15%. Read more on this condition which is one of the most prevalent solid tumors........... [curofy.com]
Etiology
The etiology remains unknown. [humpath.com]
The etiology remains unknown. We describe two patients with anomalies consistent with the Sakoda complex including the cardinal features of sphenoethmoidal encephalomeningocele and cleft palate. [pubmed.ncbi.nlm.nih.gov]