Johnson–McMillin syndrome
639 VIEWS
Everipedia is now IQ.wiki - Join the IQ Brainlist and our Discord for early access to editing on the new platform and to participate in the beta testing.
Johnson–McMillin syndrome
Johnson–McMillin syndrome
Johnson–McMillin syndrome | |
---|---|
Other names | Alopecia-anosmia-deafness-hypogonadism syndrome |
Johnson–McMillin syndrome is inherited in an autosomal dominant manner |
Johnson–McMillin syndrome is a neuroectodermal syndrome that consist of conductive hearing loss and microtia.[1]
Johnson–McMillin syndrome | |
---|---|
Other names | Alopecia-anosmia-deafness-hypogonadism syndrome |
Johnson–McMillin syndrome is inherited in an autosomal dominant manner |
See also
List of cutaneous conditions
References
[1]
Citation Linkopenlibrary.orgRapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. p. 831. ISBN 1-4160-2999-0.
Sep 22, 2019, 6:39 AM
[8]
Citation Linken.wikipedia.orgThe original version of this page is from Wikipedia, you can edit the page right here on Everipedia.Text is available under the Creative Commons Attribution-ShareAlike License.Additional terms may apply.See everipedia.org/everipedia-termsfor further details.Images/media credited individually (click the icon for details).
Sep 22, 2019, 6:39 AM