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Otofaciocervical syndrome(OFC)

MedGen UID:
322257
Concept ID:
C1833691
Disease or Syndrome
Synonyms: Familial oto-facio-cervical dysmorphia; Fara Chlupackova syndrome; OFC
SNOMED CT: Otofaciocervical syndrome (763860004); Fara Chlupackova syndrome (763860004)
 
Monarch Initiative: MONDO:0008163
OMIM® Phenotypic series: PS166780
Orphanet: ORPHA2792

Definition

A rare genetic developmental defect during embryogenesis with characteristics of distinct facial features (long triangular face, broad forehead, narrow nose and mandible, high arched palate), prominent, dysmorphic ears (low-set and cup-shaped with large conchae and hypoplastic tragus, antitragus and lobe), long neck, preauricular and/or branchial fistulas and/or cysts, hypoplastic cervical muscles with sloping shoulders and clavicles, winged, low, and laterally-set scapulae, hearing impairment and mild intellectual deficit. Vertebral defects and short stature may also be associated. [from SNOMEDCT_US]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVOtofaciocervical syndrome

Recent clinical studies

Therapy

Kreins AY, Bonfanti P, Davies EG
Front Immunol 2021;12:655354. Epub 2021 Mar 18 doi: 10.3389/fimmu.2021.655354. PMID: 33815417Free PMC Article

Prognosis

Pohl E, Aykut A, Beleggia F, Karaca E, Durmaz B, Keupp K, Arslan E, Palamar M, Yigit G, Özkinay F, Wollnik B
Hum Genet 2013 Nov;132(11):1311-20. Epub 2013 Jul 13 doi: 10.1007/s00439-013-1337-9. PMID: 23851939

Clinical prediction guides

Salinas-Torres VM, Salinas-Torres RA
Int J Pediatr Otorhinolaryngol 2016 Jun;85:19-21. Epub 2016 Mar 22 doi: 10.1016/j.ijporl.2016.03.021. PMID: 27240490
Pohl E, Aykut A, Beleggia F, Karaca E, Durmaz B, Keupp K, Arslan E, Palamar M, Yigit G, Özkinay F, Wollnik B
Hum Genet 2013 Nov;132(11):1311-20. Epub 2013 Jul 13 doi: 10.1007/s00439-013-1337-9. PMID: 23851939

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