Literature DB >> 11336448

A new syndrome: heart defects, laryngeal anomalies, preaxial polydactyly, and colonic aganglionosis in sibs.

T Huang1, E R Elias, J B Mulliken, D J Kirse, L B Holmes.   

Abstract

We present two siblings, one male and one female, who have heart defects, duplication of toes, airway anomalies, and aganglionosis. The brother also has a bilateral complete cleft lip and palate. His airway anomalies include short epiglottis and aryepiglottic folds, which are different from his sister who has a bifid epiglottis with a central epiglottic mass. Both siblings have had some developmental delay. This constellation of anomalies appears to be unique and may represent a new autosomal recessive disorder.

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Year:  1999        PMID: 11336448     DOI: 10.1097/00125817-199903000-00008

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  3 in total

Review 1.  Hirschsprung disease, associated syndromes, and genetics: a review.

Authors:  J Amiel; S Lyonnet
Journal:  J Med Genet       Date:  2001-11       Impact factor: 6.318

Review 2.  The contribution of associated congenital anomalies in understanding Hirschsprung's disease.

Authors:  S W Moore
Journal:  Pediatr Surg Int       Date:  2006-03-04       Impact factor: 1.827

3.  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
  3 in total

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