Freeman-Sheldon Syndrome: Report of Two Cases in a Family / 대한정형외과학회잡지
The Journal of the Korean Orthopaedic Association
; : 937-941, 1996.
Article
en Ko
| WPRIM
| ID: wpr-769922
Biblioteca responsable:
WPRO
ABSTRACT
Freeman-Sheldon Syndrome is one of the very rare genetic diseases which primarily affects face, hands and feet. At first, Freeman and Sheldon described this syndrome as cranio-carpo-tarsal dystrophy in 1938 and later Burian, as "whistling face" syndrome in 1963. There were 60 cases of reports in the world up to now, and only one paper with 5 cases in a family was reported in Korea. The authors report 2 cases of Freeman-Sheldon Syndrome associated with bilateral inguinal hernias and undescended tests in a family, briefly review the literature and alert orthopaedic surgeons to this condition.
Palabras clave
Texto completo:
1
Base de datos:
WPRIM
Asunto principal:
Criptorquidismo
/
Cirujanos
/
Pie
/
Mano
/
Hernia Inguinal
/
Corea (Geográfico)
Límite:
Humans
/
Male
País/Región como asunto:
Asia
Idioma:
Ko
Revista:
The Journal of the Korean Orthopaedic Association
Año:
1996
Tipo del documento:
Article