JOHNSON �MCMILLIN 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.

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]

References

^ ^a ^b "OMIM Entry - % 147770 - JOHNSON NEUROECTODERMAL SYNDROME". www.omim.org. Retrieved 2019-12-24.
^ 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.
^ Abdel-Meguid, N; Gebril, OH; Abdelraouf, ER; Shafie, MA; Bahgat, M (2014). "Johnson-McMillin Microtia Syndrome: New Additional Family". J Family Med Prim Care. 3 (3): 275–8. doi: 10.4103/2249-4863.141639. PMC 4209688. PMID 25374870.

This Genodermatoses article is a stub. You can help Wikipedia by expanding it.

Classification	D ICD- 10: Q87.8 OMIM: 147770 MeSH: C535882
External resources	Orphanet: 2316

Classification	D ICD- 10: Q87.8 OMIM: 147770 MeSH: C535882
External resources	Orphanet: 2316

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.