Johnson–McMillin syndrome

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

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

See also

  • List of cutaneous conditions

References

  1. "OMIM Entry - % 147770 - JOHNSON NEUROECTODERMAL SYNDROME". www.omim.org. 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.







Classification
External resources
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.