Johnson–McMillin syndrome

Johnson–McMillin syndrome, also known as Johnson neuroectodermal syndrome, is a neuroectodermal syndrome characterized by alopecia, microtia, conductive hearing loss, anosmia/hyposmia, and hypogonadotropic hypogonadism.^[2][3]

Other namesJohnson neuroectodermal syndrome,^[1] alopecia–anosmia–deafness–hypogonadism syndrome^[1]

SpecialtyMedical genetics

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Johnson–McMillin syndrome
Other names	Johnson neuroectodermal syndrome,[1] alopecia–anosmia–deafness–hypogonadism syndrome[1]
Johnson–McMillin syndrome is inherited in an autosomal dominant manner.
Specialty	Medical genetics

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