Johnson–McMillin syndrome explained

Synonyms:	Johnson neuroectodermal syndrome,^[1] alopecia–anosmia–deafness–hypogonadism syndrome
Johnson–McMillin syndrome
Field:	Medical genetics

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]}

See also

• List of cutaneous conditions

Notes and References

1. Web site: OMIM Entry - % 147770 - JOHNSON NEUROECTODERMAL SYNDROME. www.omim.org. 2019-12-24.
2. Book: Rapini, Ronald P. . Bolognia, Jean L. . Jorizzo, Joseph L. . Dermatology: 2-Volume Set . Mosby . St. Louis . 2007 . 831 . 978-1-4160-2999-1 .
3. Abdel-Meguid . N . Nagwa Abdel Meguid . 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 . 10.4103/2249-4863.141639 . 4209688 . 25374870 . free .