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 names | Johnson neuroectodermal syndrome,[1] alopecia–anosmia–deafness–hypogonadism syndrome[1] |
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| Johnson–McMillin syndrome is inherited in an autosomal dominant manner. | |
See also
- List of cutaneous conditions
References
- "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.
External links
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| External resources |
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