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Czasopismo

2013 | 72 | 4 |

Tytuł artykułu

A rare case of Goldenhar syndrome with radial aplasia

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Goldenhar syndrome (GS) is a well-recognised condition characterised by variable degree of uni- or bilateral involvement of craniofacial structures involving first and second branchial arches manifesting ocular and auricular anomalies and also vertebral defect. This syndrome presents at birth and its exact aetiology is still unknown. The affections of the neural crest cells may have some role in the multiple malformations of the GS. We present a teenaged female case who attended the Orthopaedic Outpatient Department to receive handicapped certificate in Bankura Sammilani Medical College and Hospital. She had multiple skeletal abnormalities, which included hemifacial microsomia, vertebral malformations in the form of scoliosis, distorted pelvis, but the most striking feature was the absence of thumb and aplasia of radius of left side. She did not suffer from any ocular or auricular abnormalities, neither from any cardiological, urogenital or gastroenteric ones. Radial defects associated with GS might represent a subset within this spectrum. Our case probably belongs to this subset, therefore is a very rare one. (Folia Morphol 2013; 72, 4: 362–365)

Wydawca

-

Czasopismo

Rocznik

Tom

72

Numer

4

Opis fizyczny

p.362-365,fig.,ref.

Twórcy

autor
  • Department of Anatomy, N.R.S.Medical College, Kolkata, India
autor
  • Depatment of Pharmacology, R.G.Kar Medical College, Kolkata, India
autor
  • Department of Anatomy, R.G.Kar Medical College, Kolkata, India
autor
  • Department of Anatomy, Bankura Sammilani Medical College, India

Bibliografia

  • 1. Anderson PJ, David DJ (2005) Spinal anomalies in Goldenhar syndrome. Cleft Palate Craniofac J, 42: 477–480.
  • 2. Avon SW, Shively JL (1988) Orthopaedic manifestations of Goldenhar syndrome. J Pediatr Orthop, 6: 683–686.
  • 3. Cazabon S, Bradbury JA (2003) Ocular coloboma and radial aplasia:syndrome or association. Eye, 17: 532–534.
  • 4. Cetinkaya M, Ozkan H, Köksal N (2008) Unilateral radius aplasia due to lamotrigine and oxcarbazepine use in pregnancy. J Matern Fetal Neonatal Med, 21: 927–930.
  • 5. Cohen MM Jr, Rollnick BR, Kaye CI (1989) Oculoauriculovertebral spectrum: an updated critique. Cleft Palate J, 26: 276–286.
  • 6. Digilio M C, Giannotti A, MarinoB, Guadagni A M, Orzalesi M, Dallapiccola B (1997) Radial aplasia and chromosome 22ql 1 deletion. J Med Genet, 34: 942–944.
  • 7. Martelli H Jr, Miranda RT, Fernandes CM, Bonan PR, Paranaíba LM, Graner E, Coletta RD (2010) Goldenhar syndrome: clinical features with orofacial emphasis. J Appl Oral Sci, 18: 646–649.
  • 8. Rollnick BR, Kaye CI, Nagatoshi K, Hauck W, Martin AO (1987) Oculoauriculovertebral dysplasia and variants: phenotypic characteristics of 294 patients. Am J Med Genet, 26: 361–375.
  • 9. Stromland K, Miller M, Sjogreen L, Johansson M, Joelsson BM, Billstedt E (2007) Oculo-auriculo-vertebral spectrum: associated factors. Am J Med Genet A, 143A: 1317–1325.
  • 10. Tasse C, Bohringer S, Fischer S, Ludecke HJ, Albrecht B, Horn D, Janecke A, Kling R, Konig R, Lorenz B, Majewski F, Maeyens E, Meinecke P, Mitulla B, Mohr C, Preischl M, Umstadt H, Kohlhase J, Gillessen-Kaesbach G, Wieczorek D (2005) Oculo-auriculo-vertebral spectrum (OAVS): clinical evaluation and severity scoring of 53 patients and proposal for a new classification. Eur J Med Genet, 48: 397–411.
  • 11. Touliatou V, Fryssira H, Mavrou A, Kanavakis E, Kitsiou-Tzeli S (2006) Clinical manifestations in 17 Greek patients with Goldenhar syndrome. Genet Couns, 17: 359–370.
  • 12. Vendramini S, Richieri-Costa A, Guion-Almeida ML (2007) Oculoauriculovertebral spectrum with radial defects: a new syndrome or an extension of the oculoauriculovertebral spectrum? Report of fourteen Brazilian cases and review of the literature. Eur J Human Gen, 15: 411–421.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

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