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Johnson–McMillin syndrome

Field	Value
synonyms	Johnson neuroectodermal syndrome, alopecia–anosmia–deafness–hypogonadism syndrome
name	Johnson–McMillin syndrome
image	Autosomal dominant - en.svg
image_size	150px
caption	Johnson–McMillin syndrome is inherited in an autosomal dominant manner.
field	Medical genetics

Johnson–McMillin syndrome, also known as Johnson neuroectodermal syndrome, is a neuroectodermal syndrome characterized by alopecia, microtia, conductive hearing loss, anosmia/hyposmia, and hypogonadotropic hypogonadism.

References

"OMIM Entry - % 147770 - JOHNSON NEUROECTODERMAL SYNDROME".
Rapini, Ronald P.. (2007). "Dermatology: 2-Volume Set". Mosby.
Abdel-Meguid. (2014). "Johnson-McMillin Microtia Syndrome: New Additional Family.". J Family Med Prim Care.

Info: Wikipedia Source

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genodermatoses genetic-disorders-with-omim-but-no-gene syndromes-affecting-hearing rare-genetic-syndromes

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