Roberts Syndrome: A case report
Journal of the Korean Academy of Rehabilitation Medicine
;
: 352-354, 2002.
Artigo
em Coreano
| WPRIM
| ID: wpr-723629
ABSTRACT
Roberts syndrome is a rare genetic disorder characterized by pre- and postnatal growth retardation, symmetrical limb defects and craniofacial anomalies. A report is given on a 5 year old male child showing the following anomalies; bilateral aplasia of distal humerus, radius, ulnar and 5th midphalanx of hand, cleft palate, hypertelorism and craniosynostosis, pronated foot with genu valgus. We report one case of Roberts syndrome with review of literature.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Rádio (Anatomia)
/
Fissura Palatina
/
Craniossinostoses
/
Extremidades
/
Pé
/
Mãos
/
Úmero
/
Hipertelorismo
Limite:
Criança
/
Criança, pré-escolar
/
Humanos
/
Masculino
Idioma:
Coreano
Revista:
Journal of the Korean Academy of Rehabilitation Medicine
Ano de publicação:
2002
Tipo de documento:
Artigo
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