Aromatase excess syndrome presenting with prepubertal gynecomastia in an Egyptian child with type 1 neurofibromatosis.
dc.contributor.author | Metwalley, Kotb Abbass | |
dc.contributor.author | Farghaly, Hekma Saad | |
dc.date.accessioned | 2015-03-05T10:26:28Z | |
dc.date.available | 2015-03-05T10:26:28Z | |
dc.date.issued | 2013-10 | |
dc.description.abstract | A romatase excess syndrome (AEXS) is a rare autosomal dominant disorder characterized by prepubertal gynecomastia, it responds well to medical treatment. In the absence of prompt suspicion, it can expose the patient to the risk of unnecessary surgical intervention. Up to our best knowledge, the association between AEXS and neurofibromatosis type 1 (NF1) was not reported before. Here, we describe a AEXS presenting with prepubertal gynecomastia in an Egyptian child with NF1 that improved with aromatase inhibitors. | en_US |
dc.identifier.citation | Metwalley Kotb Abbass, Farghaly Hekma Saad. Aromatase excess syndrome presenting with prepubertal gynecomastia in an Egyptian child with type 1 neurofibromatosis. Indian Journal of Human Genetics. 2013 Oct-Dec ;19 (4): 472-474. | en_US |
dc.identifier.uri | https://imsear.searo.who.int/handle/123456789/156617 | |
dc.language.iso | en | en_US |
dc.source.uri | https://www.ijhg.com/article.asp?issn=0971-6866;year=2013;volume=19;issue=4;spage=472;epage=474;aulast=Metwalley | en_US |
dc.subject | Aromatase excess syndrome | en_US |
dc.subject | neurofibromatosis | en_US |
dc.subject | prepubertal gynecomastia | en_US |
dc.subject.mesh | Aromatase --genetics | |
dc.subject.mesh | Child, Preschool | |
dc.subject.mesh | Egypt --epidemiology | |
dc.subject.mesh | Gynecomastia --epidemiology | |
dc.subject.mesh | Gynecomastia --etiology | |
dc.subject.mesh | Gynecomastia --genetics | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Male | |
dc.subject.mesh | Neurofibromatoses --epidemiology | |
dc.subject.mesh | Neurofibromatoses --genetics | |
dc.title | Aromatase excess syndrome presenting with prepubertal gynecomastia in an Egyptian child with type 1 neurofibromatosis. | en_US |
dc.type | Article | en_US |