Please use this identifier to cite or link to this item: http://dl.umsu.ac.ir/handle/Hannan/155366
Title: Neuroblastoma in a Child With Wolf-Hirschhorn Syndrome.
Authors: Ozcan, Alper;Acer, Hamit;Ciraci, Saliha;Gumus, Hakan;Karakukcu, Musa;Patiroglu, Turkan;Ozdemir, Mehmet a;Unal, Ekrem
subject: Medical Science
Year: 2017
Publisher: ASCRS and ESCRS
Abstract: Neuroblastoma is the most common extracranial solid tumor of childhood originating from sympathetic nervous system cells. Neuroblastoma has also been diagnosed in conjunction with other congenital conditions such as Hirschsprung's disease, congenital hypoventilation disorder, and neurofibromatosis type 1. Wolf-Hirschhorn syndrome is a congenital disorder caused by microdeletion of short arm of chromosome 4 encoding MSX1 gene with characteristic facial features. We describe a child with dysmorphic features, developmental delay, mental retardation who developed neuroblastoma at 2 years of age and cytogenetic analysis of blood lymphocytes revealed an interstitial deletion of 4p(15,2). To best our knowledge, this report is the first report of neuroblastoma in a child with Wolf-Hirschhorn syndrome; and the reported association may be an important clue for oncological follow-up of patients with Wolf-Hirschhorn syndrome.
URI: http://linkinghub.elsevier.com/retrieve/pii/S0886335017300354
http://dl.umsu.ac.ir/handle/Hannan/155366
ISSN: 
volume: Volume 43
issue: Issue 2
month: February
Appears in Collections:Journal of Cataract- refractive surgery 2017

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