Johnson–McMillin syndrome

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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.

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

Left sided microtia and atresia of left auditory canal

See also


  1. 1.0 1.1 "OMIM Entry - % 147770 - JOHNSON NEUROECTODERMAL SYNDROME". Archived from the original on 2019-12-24. Retrieved 2019-12-24.
  2. Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. p. 831. ISBN 978-1-4160-2999-1.

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