[Sturge-Weber syndrome: a case study]. 1980

N Tatematsu, and Y Uesugi, and S Shu, and M Kojima, and H Fukui

UI MeSH Term Description Entries
D005260 Female Females
D005887 Gingival Neoplasms New abnormal growth of tissue in the GINGIVA. Epulis, Congenital,Congenital Epulides,Congenital Epulis,Epulides, Congenital,Neoplasms, Gingival,Gingival Neoplasm,Neoplasm, Gingival
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults
D000798 Angiomatosis A condition with multiple tumor-like lesions caused either by congenital or developmental malformations of BLOOD VESSELS, or reactive vascular proliferations, such as in bacillary angiomatosis. Angiomatosis is considered non-neoplastic. Angiomatoses
D013341 Sturge-Weber Syndrome A non-inherited congenital condition with vascular and neurological abnormalities. It is characterized by facial vascular nevi (PORT-WINE STAIN), and capillary angiomatosis of intracranial membranes (MENINGES; CHOROID). Neurological features include EPILEPSY; cognitive deficits; GLAUCOMA; and visual defects. Neuroretinoangiomatosis,Phakomatosis, Sturge-Weber,Angiomatosis Oculoorbital-Thalamic Syndrome,Encephalofacial Hemangiomatosis Syndrome,Meningo-Oculo-Facial Angiomatosis,Meningofacial Angiomatosis-Cerebral Calcification Syndrome,Parkes Weber Syndrome,Parkes-Weber Syndrome,Sturge Disease,Sturge Syndrome,Sturge's Syndrome,Sturge-Kalischer-Weber Syndrome,Sturge-Weber-Dimitri Syndrome,Sturge-Weber-Krabbe Syndrome,Angiomatosis, Meningo-Oculo-Facial,Hemangiomatosis Syndrome, Encephalofacial,Meningo Oculo Facial Angiomatosis,Phakomatosis, Sturge Weber,Sturge Kalischer Weber Syndrome,Sturge Weber Dimitri Syndrome,Sturge Weber Krabbe Syndrome,Sturge Weber Syndrome,Sturge-Weber Phakomatosis,Syndrome, Encephalofacial Hemangiomatosis,Syndrome, Parkes Weber,Syndrome, Parkes-Weber,Syndrome, Sturge,Syndrome, Sturge's,Syndrome, Sturge-Kalischer-Weber,Syndrome, Sturge-Weber,Syndrome, Sturge-Weber-Dimitri,Syndrome, Sturge-Weber-Krabbe

Related Publications

N Tatematsu, and Y Uesugi, and S Shu, and M Kojima, and H Fukui
May 2017, Journal of clinical and diagnostic research : JCDR,
N Tatematsu, and Y Uesugi, and S Shu, and M Kojima, and H Fukui
April 2014, Advances in neonatal care : official journal of the National Association of Neonatal Nurses,
N Tatematsu, and Y Uesugi, and S Shu, and M Kojima, and H Fukui
January 2006, Neonatal network : NN,
N Tatematsu, and Y Uesugi, and S Shu, and M Kojima, and H Fukui
July 2010, Contemporary clinical dentistry,
N Tatematsu, and Y Uesugi, and S Shu, and M Kojima, and H Fukui
January 2008, Journal of the Indian Society of Pedodontics and Preventive Dentistry,
N Tatematsu, and Y Uesugi, and S Shu, and M Kojima, and H Fukui
January 1971, Pediatria polska,
N Tatematsu, and Y Uesugi, and S Shu, and M Kojima, and H Fukui
January 2015, Journal of oral biology and craniofacial research,
N Tatematsu, and Y Uesugi, and S Shu, and M Kojima, and H Fukui
November 2023, JNMA; journal of the Nepal Medical Association,
N Tatematsu, and Y Uesugi, and S Shu, and M Kojima, and H Fukui
January 2020, The Pan African medical journal,
N Tatematsu, and Y Uesugi, and S Shu, and M Kojima, and H Fukui
January 1965, Klinika oczna,
Copied contents to your clipboard!