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Early Onset Cerebral Infarction in Schimke Immuno-Osseous Dysplasia.
Hossein Babaei, Amir; Inaloo, Soroor; Basiratnia, Mitra; Derakhshan, Ali.
Afiliação
  • Hossein Babaei A; Medical Student, Student Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Inaloo S; Department of Pediatric Neurology, Neonatal Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Basiratnia M; Department of Pediatrics Nephrology, Shiraz Nephrology-Urology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Derakhshan A; Department of Pediatrics Nephrology, Shiraz Nephrology-Urology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Iran J Child Neurol ; 12(3): 126-132, 2018.
Article em En | MEDLINE | ID: mdl-30026777
Schimke Immuno-osseous Dysplasia (SIOD) is a rare autosomal recessive disease caused by a biallelic mutation in SMARCAL1 gene. Typical findings in SIOD include spondylo-epiphyseal dysplasia, steroid resistance nephrotic syndrome, progressive renal failure, T-cell immunodeficiency, bone marrow failure, and cerebral infarction. In this case report, we describe a 9-yr-old girl who presented with failure to thrive in infancy. Nephrotic syndrome was diagnosed at the age of four years. She had three episodes of admission with cerebral stroke due to moyamoya syndrome. In the last admission at Namazi Hospital, Shiraz, southern Iran, in October 2016, she had new cerebral ischemia, developed seizure, and finally died.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article