Johnson–McMillin syndrome

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Johnson–McMillin syndrome
Other namesJohnson neuroectodermal syndrome,[1] alopecia–anosmia–deafness–hypogonadism syndrome[1]
Autosomal dominant - en.svg
Johnson–McMillin syndrome is inherited in an autosomal dominant manner.

Johnson–McMillin syndrome, also known as Johnson neuroectodermal syndrome, is a neuroectodermal syndrome that consists of conductive hearing loss and microtia.[2]

See also

References

  1. 1.0 1.1







External links

Classification
External resources
 

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