Type IV Laryngotracheoesophageal Cleft Associated with Type III Esophageal Atresia in 1p36 Deletions Containing the RERE Gene: Is There a Causal Role for the Genetic Alteration?
The causes of embryological developmental anomalies leading to laryngotracheoesophageal clefts (LTECs) are not known, but are proposed to be multifactorial, including genetic and environmental factors. Haploinsufficiency of the RERE gene might contribute to different phenotypes seen in individuals w...
Main Authors: | Gloria Pelizzo, Aurora Puglisi, Maria Lapi, Maria Piccione, Federico Matina, Martina Busè, Giovanni Battista Mura, Giuseppe Re, Valeria Calcaterra |
---|---|
Format: | Article |
Language: | English |
Published: |
Hindawi Limited
2018-01-01
|
Series: | Case Reports in Pediatrics |
Online Access: | http://dx.doi.org/10.1155/2018/4060527 |
Similar Items
-
Congenital laryngotracheoesophageal cleft masquerading as recurrent pneumonia
by: Vishrutha, et al.
Published: (2015-01-01) -
Laryngotracheoesophageal Cleft Type 3 and Severe Laryngotracheomalacia; Delayed Surgical Repair, a Treatment Challenge with an Excellent Outcome
by: Ahmad Khaleghnejad, et al.
Published: (2018-01-01) -
Taku Maukura e Rere Rā
by: King, JS
Published: (2011) -
An allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletions.
by: Bum Jun Kim, et al.
Published: (2013-01-01) -
Leopardi rere les traces de Montaigne
by: Franco D'Intino
Published: (2017-12-01)