Dermatology · Dermatology / Ectodermal dysplasias
Ectrodactyly–ectodermal dysplasia–clefting syndrome
also: EEC syndrome
Split hand and foot, ectodermal dysplasia and orofacial clefts.
- 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
- EEC syndrome
Etiology & mechanism
Dominant-negative p63 mutations.
Gene(s) involved (1)
Symptoms & signs (6)
In plain terms, someone with Ectrodactyly–ectodermal dysplasia–clefting 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.
Drag nodes, scroll to zoom, click a node to open that syndrome.
Shares symptoms with
3 shared
Hypohidrotic ectodermal dysplasia
hypodontia, hypohidrosis, sparse hair
3 shared
Rapp–Hodgkin syndrome
cleft lip and palate, hypodontia, hypohidrosis
2 shared
Hay–Wells syndrome
hypodontia, sparse hair
1 shared
Bazex–Dupré–Christol syndrome
hypohidrosis
1 shared
Cardiofaciocutaneous syndrome
sparse hair
1 shared
Fetal hydantoin syndrome
cleft lip and palate
1 shared
Langer–Giedion syndrome
sparse hair
1 shared
Laron syndrome
sparse hair
1 shared
Naegeli–Franceschetti–Jadassohn syndrome
hypohidrosis
1 shared
Nicolaides–Baraitser syndrome
sparse hair
Shares genes with
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