Ciliopathy with craniosynostosis, ectodermal anomalies and nephronophthisis.
- Specialty
- Genetics
- Subspecialty
- Genetics / Ciliopathies
- Sex & age distribution
- Male: affected; Female: affected, equal; Children: yes
- Gene(s) involved
- IFT122, IFT43, IFT52, WDR19, WDR35
- Alternative names & eponyms
- Cranioectodermal dysplasia
Etiology & mechanism
Intraflagellar transport defect.
Gene(s) involved (5)
Symptoms & signs (6)
In plain terms, someone with Sensenbrenner 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
1 shared
Apert syndrome
craniosynostosis
1 shared
Cardiofaciocutaneous syndrome
sparse hair
1 shared
Crouzon syndrome
craniosynostosis
1 shared
Ectrodactyly–ectodermal dysplasia–clefting syndrome
sparse hair
1 shared
Ellis–van Creveld syndrome
short limbs
1 shared
Hay–Wells syndrome
sparse hair
1 shared
Hypohidrotic ectodermal dysplasia
sparse hair
1 shared
Jeune syndrome
narrow thorax
1 shared
Langer–Giedion syndrome
sparse hair
1 shared
Laron syndrome
sparse hair
Shares genes with
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