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Noonan syndrome with leukaemoid reaction and overproduction of catecholamines: a case report

✍ Scribed by Tatsuro Kondoh; Eiich Ishii; Yoko Aoki; Takashi Shimizu; Masafumi Zaitsu; Yoichi Matsubara; Hiroyuki Moriuchi


Publisher
Springer
Year
2003
Tongue
English
Weight
151 KB
Volume
162
Category
Article
ISSN
0340-6997

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## Abstract ## BACKGROUND Johnson‐McMillin syndrome (JMS) is a rare neuroectodermal disorder characterized by alopecia, ear malformations, conductive hearing loss, anosmia/hyposmia, and hypogonadotropic hypogonadism. It is inherited in an autosomal dominant manner; however, the causative gene has