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Johnson–McMillin syndrome
Other names	Johnson neuroectodermal syndrome, alopecia–anosmia–deafness–hypogonadism syndrome
Johnson–McMillin syndrome is inherited in an autosomal dominant manner.
Specialty	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.

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.
3. 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.

External links

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• Genodermatoses
• Genetic disorders with OMIM but no gene
• Syndromes affecting hearing
• Rare genetic syndromes
• Genodermatoses stubs