Johnson_neuroectodermal_syndrome

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

Johnson–McMillin syndrome

Medical condition

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

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Johnson–McMillin syndrome

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