Microtia, severe micrognathia and absent ossicles: Auriculo-condylar syndrome or new entity?

Clinical Dysmorphology

Volumn 16, Issue 1, 2007, Pages 9-13

  Nezarati, Marjan M ^a   Aftimos, Salim ^a  

^a AUCKLAND CITY HOSPITAL   (New Zealand)

Author keywords

Auriculo condylar syndrome; Branchial arch anomalies; Microtia

Indexed keywords

ADULT; ARTICLE; AUDITORY OSSICLE; AURICULOCONDYLAR SYNDROME; BONE REMODELING; BRANCHIAL ARCH; CASE REPORT; CLEFT PALATE; CLINICAL FEATURE; CONSANGUINEOUS MARRIAGE; DIFFERENTIAL DIAGNOSIS; GOLDENHAR SYNDROME; HEARING AID; HUMAN; MALE; MANDIBULOFACIAL DYSOSTOSIS; MICROGNATHIA; MICROTIA; MIDDLE EAR MALFORMATION; NAGER ACROFACIAL DYSOSTOSIS; PALATE MALFORMATION; PALPEBRAL FISSURE ANOMALY; PRIORITY JOURNAL; SYMPTOM;

ADOLESCENT; CHOANAL ATRESIA; DIAGNOSIS, DIFFERENTIAL; HUMANS; MALE; MANDIBULOFACIAL DYSOSTOSIS; MICROGNATHISM; PEDIGREE;

EID: 33845646217     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/MCD.0b013e3280110b57     Document Type: Article

References (14)

1. Baker PA, Aftimos S, Anderson BJ (2004). Airway management during an EXIT procedure for a fetus with dysgnathia complex. Pediatr Anesth 14:781-786.
2. Divizia MT, Cordone A, Bado M, Rosaia L, Cirillo Silengo M, Ravazzolo R, Lerone M. (2002). Auriculo-condylar syndrome or new syndrome. Clin Dysmorphol 11:143-144.
3. Erlich MS, Cunningham ML, Hudgins L (2000). Transmission of the dysgnathia complex from mother to daughter. Am J Med Genet 95:269-274.
4. Gorlin RJ, Jue KL, Jacobsen V, Goldschmidt E (1963). Oculoauriculovertebral dysplasia. J Pediatr 63:991-999.
5. Guion-Almeida ML, Kokitsu-Nakata NM, Zechi-Ceide RM, Vendramini S (1999). Auriculo-condylar syndrome: further evidence for a new disorder. Am J Med Genet 86:130-133.
6. Guion-Almeida ML, Zechi-Ceide RM, Vendramini S, Kokitsu-Nakata NM (2002). Auriculo-condylar syndrome: additional patients. Am J Med Genet 112:209-214.
7. Jampol M, Repetto G, Keith DA, Curtin H, Remensnyder J, Holmes LB (1998). Prominent, constricted ears with malformed condyle of the mandible. Am J Med Genet 74:449-452.
8. Kaye CI, Rollnick BR, Hauck WW, Martin AO, Richmaster JT, Nagatoshi K (1989). Microtia and associated anomalies: statistical analysis. Am J Med Genet 34:574-578.
9. Marres HA, Cremers CW, Dixon MJ, Huygen PL, Joosten FB (1995). The Treacher Collins syndrome. A clinical, radiological, and genetic linkage study on two pedigrees. Arch Otolaryngol Head Neck Surg 121:509-514.
10. Mastroiacovo P, Corchia A, Botto L, Lanni R, Zampino G, Fusco D (1995). Epidemiology and genetics of microtia-anotia: a registry based study on over one million births. J Med Genet 32:453-457.
11. Ozturk S, Sengezer M, Isik S, Gul D (2005). The correction of auricular and mandibular deformities in auriculo-condylar syndrome. J Craniofacial Surg 16:489-492.
12. Priolo M, Lerone M, Rosaia L, Calcagno EP, Sadeghi AK, Ghezzi F, et al. (2000). Question mark ears, temporo-mandibular joint malformation and hypotonia: auriculo-condylar syndrome or a distinct entity. Clin Dysmorphol 9:277-280.
13. Shermak MA, Dufresne CR (1996). Nonlethal case of otocephaly and its implications for treatment. J Craniofacial Surg 7:372-375.
14. Storm AL, Johnson JM, Lammer E, Green GE, Cunniff C (2005). Auriculocondylar syndrome is associated with highly variable ear and mandibular defects in multiple kindreds. Am J Med Genet 138A:141-145.