Short stature, hypertelorism and gingival hyperplasia.
- Specialty
- Dentistry
- Subspecialty
- Dentistry / Oral and maxillofacial surgery
- Sex & age distribution
- Male: affected; Female: affected; Children: yes
- Gene(s) involved
- DVL1, DVL3, ROR2, WNT5A
- Alternative names & eponyms
- Fetal face syndrome
Etiology & mechanism
WNT5A or ROR2 mutation.
Gene(s) involved (4)
Symptoms & signs (4)
In plain terms, someone with Robinow 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
1 shared
Aarskog–Scott syndrome
hypertelorism
1 shared
Amelogenesis imperfecta with nephrocalcinosis syndrome
gingival hyperplasia
1 shared
Crouzon syndrome
hypertelorism
1 shared
Ellis–van Creveld syndrome
short limbs
1 shared
Kallmann syndrome
micropenis
1 shared
LEOPARD syndrome
hypertelorism
1 shared
Loeys–Dietz syndrome
hypertelorism
1 shared
Noonan syndrome
hypertelorism
1 shared
Noonan syndrome with multiple lentigines
hypertelorism
1 shared
Opitz G/BBB syndrome
hypertelorism
Shares genes with
None.
Loading…
Loading…