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pro vyhledávání: '"Selma Pamukcuoglu"'
Autor:
Selma Pamukcuoglu, Arzu Okur, Ayse Gul Alimli, Oznur Boyunaga, Alp Özgün Börcek, Cigdem Oztunali
Publikováno v:
The Neuroradiology Journal. 29:146-149
Isolated intracranial Rosai–Dorfman disease (RDD) is extremely rare in pediatric patients. We present the case of a 22-month-old boy whom had isolated intracranial RDD involvement. To our knowledge, a parieto-occipital regional involvement without
Publikováno v:
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. 33(1)
Smith-Lemli-Opitz Syndrome (SLOS) is a rare hereditary autosomal recessive disorder with broken cholesterol synthesis causing by 7-dehydrocholesterol reductase deficiency. Although the clinical features and pathogenesis is well-defined, it is unknown