Robinow syndrome

Also known as: Fetal face syndrome

Short stature, hypertelorism and gingival hyperplasia.

Medical specialty: Dentistry
Subspecialty: Dentistry / Oral and maxillofacial surgery
Sex & age distribution: Male: affected; Female: affected; Children: yes
Gene(s) involved: DVL1, DVL3, ROR2, WNT5A

Etiology & mechanism

WNT5A or ROR2 mutation.

Gene(s) involved (4)

DVL1DVL3ROR2WNT5A

Symptoms & signs (4)

gingival hyperplasiahypertelorismmicropenisshort limbs

SyndromeScope — educational reference. Content is model-generated and not clinically verified; always confirm against OMIM, Orphanet and GeneReviews before clinical use.