Ankyloblepharon, ectodermal dysplasia and clefting.
- Specialty
- Dermatology
- Subspecialty
- Dermatology / Ectodermal dysplasias
- Sex & age distribution
- Male: affected; Female: affected, equal; Children: yes, from birth
- Gene(s) involved
- TP63
- Alternative names & eponyms
- AEC syndrome
Etiology & mechanism
Dominant-negative p63 SAM-domain mutations.
Gene(s) involved (1)
Symptoms & signs (6)
In plain terms, someone with Hay–Wells 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
Ectrodactyly–ectodermal dysplasia–clefting syndrome
hypodontia, sparse hair
2 shared
Hypohidrotic ectodermal dysplasia
hypodontia, sparse hair
2 shared
Rapp–Hodgkin syndrome
hypodontia, nail dystrophy
2 shared
Revesz syndrome
nail dystrophy, sparse hair
2 shared
Van der Woude syndrome
cleft palate, hypodontia
1 shared
Apert syndrome
cleft palate
1 shared
Bamforth–Lazarus syndrome
cleft palate
1 shared
Bazex syndrome
nail dystrophy
1 shared
Cardiofaciocutaneous syndrome
sparse hair
1 shared
Diamond–Blackfan anemia
cleft palate
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