Otomandibular syndrome

A rare, otomandibular dysplasia characterized by asymmetric, predominantly unilateral hypoplasia of facial structures, typically involving the external ear, mandible, and ipsilateral facial soft tissues. It manifests with mild to severe facial asymmetry, micrognathia, microtia, slanted lip commissure and occlusal canting.

Cleft lip

A gap in the lip or lips.


Total: 2

                       


(per page)
PMID (PMCID)
25664313
(4317524)
 OTHER
Sequential treatment for a patient with hemifacial microsomia: 10 year-long term follow up.
Seo JS, Roh YC, Song JM, Song WW, Seong HS, Kim SY, Hwang DS, Kim UK.
Maxillofac Plast Reconstr Surg. 2015;37(1):3.
Hemifacial microsomia (HFM) is the most common craniofacial anomaly after cleft lip and cleft palate; this deformity primarily involves the facial skeleton and ear, with either underdevelopment or absence of both components.
18292629
(2636090)
 MALE Infant
A case of Goldenhar-Gorlin syndrome with unusual association of hypoplastic thumb.
Das A, Ray B, Das D, Das S.
Indian J Ophthalmol. 2008;56(2):150-2.
Hemifacial microsomia was unilateral and was associated with cleft lip, macrostomia, dental misalignment, large tongue and high arched palate.