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Literature DB >> 17558506

H-type tracheoesophageal fistula with type III laryngotracheoesophageal cleft.

Brice Antao¹, Giampiero Soccorso, Neil Bateman, Rang Shawis.

Abstract

H-type tracheoesophageal fistula and laryngotracheoesophageal cleft are both rare anomalies. Laryngotracheoesophageal clefts are identified as a part of Opitz-Frias syndrome. We report a neonate with this combination of rare congenital anomalies. These associated malformations can have major implications in terms of resuscitation, diagnosis and surgical management, which are discussed.

Entities: Disease

Mesh：

Year: 2007 PMID： 17558506 DOI： 10.1007/s00405-007-0356-3

Source DB: PubMed Journal: Eur Arch Otorhinolaryngol ISSN： 0937-4477 Impact factor: 2.503

16 in total

1. Concurrent type 1 laryngotracheoesophageal cleft and H-type tracheoesophageal fistula.

Authors: T E Herman; M J Siegel
Journal: J Perinatol Date: 2001 Jul-Aug Impact factor: 2.521

2. Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2.

Authors: N H Robin; G J Feldman; A L Aronson; H F Mitchell; R Weksberg; C O Leonard; B K Burton; K D Josephson; R Laxová; K A Aleck; J E Allanson; M L Guion-Almeida; R A Martin; L G Leichtman; R A Price; J M Opitz; M Muenke
Journal: Nat Genet Date: 1995-12 Impact factor: 38.330

H-type tracheoesophageal fistula with type III laryngotracheoesophageal cleft.

1. Concurrent type 1 laryngotracheoesophageal cleft and H-type tracheoesophageal fistula.

2. Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2.

3. Fatal aspirations in infancy during gastrointestinal series.

4. Laryngo-tracheo-oesophageal cleft. Clinical features, diagnosis and therapy.

5. Management and long-term follow-up of patients with types III and IV laryngotracheoesophageal clefts.

6. Management of the isolated congenital tracheo-oesophageal fistula.

7. Laryngotracheoesophageal clefts.

8. Does the presence of a tracheoesophageal fistula predict the outcome of laryngeal cleft repair?

9. H-type tracheoesophageal fistula and congenital esophageal stenosis.

10. The G and BBB syndromes: case presentations, genetics, and nosology.

1. Prevalence of Laryngeal Cleft in Pediatric Patients With Esophageal Atresia.

2. Diagnostic and management strategies for congenital H-type tracheoesophageal fistula: a systematic review.