Literature DB >> 8659937

Bifid epiglottis.

J D Goldenberg1, L D Holinger, F J Bressler, L R Hutchinson.   

Abstract

The true bifid epiglottis is a rare congenital anomaly typically discovered during the evaluation of stridor in an infant or newborn. While it is not classified as a specific syndrome, there are frequent associations of other congenital anomalies with the bifid epiglottis. These include midline defects (such as microphallus, hypospadius, imperforate anus, and midline laryngeal cleft), endocrine disorders (including congenital hypopituitarism), and central nervous system neoplasms, including hypothalamic hamartoblastoma. The embryogenesis and options for surgical management of this anomaly are reviewed, and one case is presented in detail.

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Mesh:

Year:  1996        PMID: 8659937     DOI: 10.1177/000348949610500211

Source DB:  PubMed          Journal:  Ann Otol Rhinol Laryngol        ISSN: 0003-4894            Impact factor:   1.547


  2 in total

1.  Linkage mapping and phenotypic analysis of autosomal dominant Pallister-Hall syndrome.

Authors:  S Kang; J Allen; J M Graham; T Grebe; C Clericuzio; N Patronas; F Ondrey; E Green; A Schäffer; M Abbott; L G Biesecker
Journal:  J Med Genet       Date:  1997-06       Impact factor: 6.318

2.  Bifid epiglottis: What perioperative physician should know about it?

Authors:  Rupesh Yadav; Sohan Lal Solanki; Jeson R Doctor
Journal:  Ann Card Anaesth       Date:  2017 Oct-Dec
  2 in total

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