Johnson–McMillin syndrome
Johnson–McMillin syndrome is a neuroectodermal syndrome that consists 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
References
- Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. p. 831. ISBN 1-4160-2999-0.
External links
| Classification | |
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| External resources |
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