Your browser doesn't support javascript.
loading
A nine-year-old patient affected by chromosomal aberration with the suspicion of juvenile idiopathic arthritis.
Zuber, Zbigniew; Nawrotek, Magdalena; Sobczyk, Malgorzata; Mezyk, Elzbieta; Turowska-Heydel, Dorota.
Afiliação
  • Zuber Z; Department of Older Children with Subunits of Neurology, Rheumatology and Rehabilitation, St. Louis Regional Specialised Children's Hospital, Krakow, Poland.
  • Nawrotek M; Department of Older Children with Subunits of Neurology, Rheumatology and Rehabilitation, St. Louis Regional Specialised Children's Hospital, Krakow, Poland.
  • Sobczyk M; Department of Older Children with Subunits of Neurology, Rheumatology and Rehabilitation, St. Louis Regional Specialised Children's Hospital, Krakow, Poland.
  • Mezyk E; Department of Older Children with Subunits of Neurology, Rheumatology and Rehabilitation, St. Louis Regional Specialised Children's Hospital, Krakow, Poland.
  • Turowska-Heydel D; Department of Older Children with Subunits of Neurology, Rheumatology and Rehabilitation, St. Louis Regional Specialised Children's Hospital, Krakow, Poland.
Reumatologia ; 56(1): 59-62, 2018.
Article em En | MEDLINE | ID: mdl-29686445
ABSTRACT
We present a case study of a 9.5-year-old girl affected by chromosome 12 aberration with the suspicion of juvenile idiopathic arthritis (JIA). All the tests performed at the hospital and the presence of a genetic disorder ledus to search for a diagnosisother than JIA. We initially diagnosed spondyloepiphyseal dysplasia tarda (SEDT), which is related to chromosome 12. Certain signs and symptoms of this disease were presented by our patient at the time of admission. After analysing all the tests and the general conditionof the patient, we were unable to confirm this diagnosis. However, it is possible that the symptoms may occur during subsequentyears and may allow confirmation of SEDT in the future.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Reumatologia Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Polônia

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Reumatologia Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Polônia