| Literature DB >> 28746941 |
Kanthi Bangalore Krishna1, Pedro Pagan2, Oscar Escobar2, Jadranka Popovic2.
Abstract
Noonan syndrome (NS) is associated with short stature. Growth hormone treatment has been FDA approved for use in these patients. Children with NS are at a higher risk of developing benign and malignant proliferative disorders, primary brain tumors being one of them. Since growth hormone therapy can worsen the tumor burden, screening with a brain MRI prior to growth hormone initiation in NS patients is strongly recommended. Here we present two NS patients who developed different primary brain tumors while being on growth hormone therapy.Entities:
Keywords: Brain tumors; Growth hormone; Noonan syndrome
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Year: 2017 PMID: 28746941 PMCID: PMC9204260 DOI: 10.1159/000479107
Source DB: PubMed Journal: Horm Res Paediatr ISSN: 1663-2818 Impact factor: 4.275