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Alopecia-anosmia-deafness-hypogonadism syndrome revisited: Report of a new case

✍ Scribed by Johnston, Kathreen ;Golabi, Mahin ;Hall, Bryan ;Ito, Melanie ;Grix, Art ;Reynolds, James F.


Publisher
John Wiley and Sons
Year
1987
Tongue
English
Weight
218 KB
Volume
26
Category
Article
ISSN
0148-7299

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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