Dermatology · Dermatology / Genodermatoses
KID syndrome
also: Keratitis–ichthyosis–deafness syndrome
Erythrokeratoderma with vascularizing keratitis and deafness.
- Specialty
- Dermatology
- Subspecialty
- Dermatology / Genodermatoses
- Sex & age distribution
- Male: affected; Female: affected, equal; Children: yes, from infancy
- Gene(s) involved
- AP1B1, GJB2, GJB6
- Alternative names & eponyms
- Keratitis–ichthyosis–deafness syndrome
Etiology & mechanism
Gain-of-function connexin 26 hemichannel mutations.
Gene(s) involved (3)
Symptoms & signs (7)
In plain terms, someone with KID syndrome may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
Other syndromes that share symptoms with this one.
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Shares symptoms with
2 shared
Olmsted syndrome
alopecia, palmoplantar keratoderma
1 shared
Autoimmune polyglandular syndrome type 1
alopecia
1 shared
Barakat syndrome
sensorineural deafness
1 shared
Brown–Vialetto–Van Laere syndrome
sensorineural deafness
1 shared
CARASIL
alopecia
1 shared
Cronkhite–Canada syndrome
alopecia
1 shared
Cyclic neutropenia syndrome
skin infections
1 shared
EAST syndrome
sensorineural deafness
1 shared
Fanconi anemia
squamous cell carcinoma
1 shared
Hutchinson–Gilford progeria syndrome
alopecia
Shares genes with
None.
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