Literature DB >> 12955254

[DiGeorge syndrome/velcardiofacial syndrome: oral and maxillofacial surgery].

W Pradel1, O Bartsch, R Müller, G Lauer, U Eckelt.   

Abstract

The DiGeorge syndrome/velocardiofacial syndrome is the most frequent chromosomal microdeletion syndrome. Partial deletion of chromosome 22q11 may lead to symptoms including facial dysmorphy, hypoparathyroidism, thymic aplasia, congenital heart disease, developmental retardation, and disturbance of speech development. According to the literature, 9% of patients have cleft palate, an additional 5% have a submucosal cleft, and a total of 32% show velopharyngeal insufficiency. We studied 64 children with a cleft, or with delayed speech development and a submucosal or occult cleft, for the presence of the 22q11deletion using fluorescent in situ hybridisation. Five patients had the 22q11 deletion. We conclude that patients presenting with nasal speech and additional anomalies should all be studied for the presence of submucosal or occult clefting and for the presence of the DiGeorge syndrome/velocardiofacial syndrome.

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Year:  2003        PMID: 12955254     DOI: 10.1007/s00106-003-0874-2

Source DB:  PubMed          Journal:  HNO        ISSN: 0017-6192            Impact factor:   1.284


  10 in total

1.  No evidence for chromosomal microdeletions at the second DiGeorge syndrome locus on 10p near D10S585.

Authors:  O Bartsch; A Wagner; G K Hinkel; P Lichtner; J Murken; S Schuffenhauer
Journal:  Am J Med Genet       Date:  1999-04-23

Review 2.  The DiGeorge anomaly as a developmental field defect.

Authors:  E J Lammer; J M Opitz
Journal:  Am J Med Genet Suppl       Date:  1986

3.  Velocardiofacial syndrome and DiGeorge sequence.

Authors:  R J Shprintzen
Journal:  J Med Genet       Date:  1994-05       Impact factor: 6.318

4.  The otolaryngologist and the patient with velocardiofacial syndrome.

Authors:  Y Finkelstein; Y Zohar; A Nachmani; Y P Talmi; M A Lerner; D J Hauben; M Frydman
Journal:  Arch Otolaryngol Head Neck Surg       Date:  1993-05

5.  Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.

Authors:  J Burn; A Takao; D Wilson; I Cross; K Momma; R Wadey; P Scambler; J Goodship
Journal:  J Med Genet       Date:  1993-10       Impact factor: 6.318

6.  DiGeorge syndrome: part of CATCH 22.

Authors:  D I Wilson; J Burn; P Scambler; J Goodship
Journal:  J Med Genet       Date:  1993-10       Impact factor: 6.318

Review 7.  Velo-cardio-facial syndrome: a review of 120 patients.

Authors:  R Goldberg; B Motzkin; R Marion; P J Scambler; R J Shprintzen
Journal:  Am J Med Genet       Date:  1993-02-01

8.  The occult submucous cleft palate.

Authors:  E N Kaplan
Journal:  Cleft Palate J       Date:  1975-10

Review 9.  DiGeorge syndrome and related syndromes associated with 22q11.2 deletions. A review.

Authors:  S Demczuk; A Aurias
Journal:  Ann Genet       Date:  1995

10.  Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.

Authors:  A K Ryan; J A Goodship; D I Wilson; N Philip; A Levy; H Seidel; S Schuffenhauer; H Oechsler; B Belohradsky; M Prieur; A Aurias; F L Raymond; J Clayton-Smith; E Hatchwell; C McKeown; F A Beemer; B Dallapiccola; G Novelli; J A Hurst; J Ignatius; A J Green; R M Winter; L Brueton; K Brøndum-Nielsen; P J Scambler
Journal:  J Med Genet       Date:  1997-10       Impact factor: 6.318

  10 in total
  1 in total

Review 1.  Update on 13 Syndromes Affecting Craniofacial and Dental Structures.

Authors:  Theodosia N Bartzela; Carine Carels; Jaap C Maltha
Journal:  Front Physiol       Date:  2017-12-14       Impact factor: 4.566

  1 in total

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