Scott-Taor Syndrome: A Clinical Case Report.
Cureus
; 16(1): e51437, 2024 Jan.
Article
em En
| MEDLINE
| ID: mdl-38169661
ABSTRACT
Scott-Taor syndrome is a benign bone dysplasia with less than 50 cases reported. The latter is an autosomal dominant disease characterized mainly by patellar a/hypoplasia and bilateral malunion ossification of the ischiopubic junction, a wide gap between the first and second toes. The diagnosis is clinical and radiographical. Here, we present a 17-year-old female patient with this rare syndrome. Considering this diagnosis is crucial for a better understanding of the pathology and to effectively contextualize the patient's clinical findings.
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Idioma:
En
Revista:
Cureus
Ano de publicação:
2024
Tipo de documento:
Article